This
is a sample written Exposure Control Plan provided
only as a guide to assist in complying with 29 CFR
1910.1030, OSHA's Bloodborne Pathogens standard.
It is not intended to supersede the
requirements detailed in the standards.
You need to review the standard for
particular requirements which are applicable to your
specific situation.
Note that this sample program does not
include provisions for HIV/HIB laboratories and
research facilities which are addressed in the
standards. If you operate this type of facility, you
need to include provisions as required by the
standard. Employers will need to delete or add
information relevant to your particular facility in
order to develop an effective, comprehensive
exposure control plan. Note that the exposure
control plan is expected to be reviewed at least on
an annual basis and updated when necessary.
This
material and safety and health consultation services
are provided at no cost to owners, proprietors, and
managers of small businesses by the Illinois Onsite
Safety & Health Consultation Program, Industrial
Services Division, Department of Commerce and
Economic Opportunity under a program funded largely by
the Occupational Safety and Health Administration (OSHA),
an agency of the U.S. Department of Labor.
ONSITE
SAFETY & HEALTH CONSULTATION PROGRAM
Illinois
Department of Commerce & Economic Opportunities
Industrial
Services Division
100
West Randolph, Suites 3-400 Chicago, Illinois 60601
Phone:
312/814-2337
Fax: 312/814-7238
TDD: 800/419-0667
BLOODBORNE
PATHOGENS EXPOSURE CONTROL PLAN
TABLE
OF CONTENTS
A.
Exposure Determination..........................................................................................................
3
B.
Implementation Schedule & Methodology..............................................................................
4
C.
Hepatitis B Vaccine & Post-Exposure Evaluation
& Follow-up
......................................
12
D.
Interaction with Health Care Professionals .........................................................................
14
E.
Information and Training .......................................................................................................
15
F.
Recordkeeping ......................................................................................................................
15
G.
Dates, Evaluation and Review .............................................................................................
17
Appendices
Statement
of Declination
Sample
Exposure Incidence Report
Sample
Training Outline
Sample
Sharps Injury Log
BLOODBORNE
PATHOGENS EXPOSURE CONTROL PLAN
FACILITY
NAME: _________________________________________
We
have developed this Exposure Control Plan (ECP) to
eliminate or minimize employee occupational
exposure to blood or other body fluids, and to
comply with OSHA’s Bloodborne Pathogens standard,
29 CFR 1910.1030. Employees covered by the
bloodborne pathogens standard receive an explanation
of this ECP during their initial training session.
It is also reviewed in their annual refresher
training. All employees have an opportunity to
review this plan at any time during their work
shifts. If requested, we will provide an employee
with a copy of the ECP free of charge and within 15
days of the request.
____________________
is the Program Administrator responsible for the
implementation of the Exposure Control Plan (ECP).
The Program Administrator will maintain, review and
update the ECP at least annually, and whenever
necessary to include new or modified tasks or
procedures. The Program Administrator is also
responsible for:
•
Maintaining
and providing all necessary personal protective
equipment (PPE), engineering controls, labels and
red bags.
•
Ensuring
that adequate supplies of equipment are available in
the appropriate sizes.
•
Ensuring
that all new recommendations or changes are
effectively implemented.
•
Ensuring
that all medical actions required are performed and
that appropriate employee health and OSHA records
are maintained.
•
Training,
documentation of training and making the written ECP
available to employees, OSHA and NIOSH
representatives.
•
Recordkeeping
A. Exposure
Determination.
Those
employees who are determined to have occupational
exposure to blood or other potentially infectious
materials (OPIM) must comply with the procedures and
work practices outlined in this ECP. The job
classifications where all employees have
occupational exposure are:
|
Job
Title
|
Department/Location
|
|
|
|
|
|
|
|
|
|
|
|
|
Job classifications where some employees have
occupational exposure is below. This list includes
all full-time, part-time, contract and per diem
employees. Included is a list of tasks and
procedures, or groups of closely related tasks and
procedures, in which occupational exposure may occur
for these individuals.
|
Job
Classification
|
Department/Location
|
Tasks/Procedures
|
|
Example:
Janitor
|
Example:
Maintenance
|
Example:
Handling Regulated Waste
|
|
|
|
|
|
|
|
|
B. Implementation Methods & Controls
1.
Universal
Precautions.
Universal precautions are used in order to prevent
contact with blood or other potentially infectious
materials (OPIM).
All blood or other potentially infectious
material are considered infectious regardless of
the perceived status of the source individual.
2.
Engineering
Controls and Work Practices. Engineering and
work practice controls are used to eliminate or
minimize exposure to employees at this facility.
Where occupational exposure remains after
institution of these controls, personal protective
equipment is also used. Specific engineering
controls and work practice controls used are listed.
Controls
listed are examined and maintained on a regular
schedule. The schedule for reviewing the
effectiveness of the controls is as follows:
We
identify the need for changes in engineering control
and work practices; we evaluate new procedures or
new products regularly. Both front line workers and
management officials are involved in this process.
Hand
washing facilities are available and readily
accessible to employees who incur exposure to
blood or other potentially infectious materials. At
this facility, hand washing facilities are located:
After
removal of personal protective gloves, employees
wash hands and any other potentially contaminated
skin area immediately or as soon as feasible with
soap and water. If employees incur exposure to their
skin or mucous membranes then those areas are washed
or flushed with water as soon as feasible following
contact.
3.
Needles
.
Contaminated needles and other contaminated sharps
will not be bent, recapped, removed, sheared or
purposely broken.
If
recapping or needle removal is required, then the
recapping or removal of the needle must be done by
the use of a mechanical device or a one_handed
technique. At
this facility recapping or removal is only permitted
for the following procedures:
4.
Containers
for Reusable Sharps
.
Contaminated sharps that are reusable are placed
after use into appropriate sharps containers. The
sharps containers are leak proof, puncture resistant
and labeled with a biohazard label.
5.
Work Area Restrictions
. Employees
may not eat, drink, apply cosmetics or lip balm,
smoke,
or handle contact lenses in any work area where
there is a reasonable likelihood of exposure to
blood or OPIM. Food and beverages are not to be kept
in refrigerators, freezers, shelves, cabinets, or on
counter tops or bench tops where blood or OPIM are
present.
All
procedures are conducted in a manner which will
minimize splashing, spraying, splattering and
generation of droplets of blood or other potentially
infectious materials. Methods which are employed to accomplish this goal are:
6.
Specimens.
Specimens of blood or OPIM are placed in a container
which prevents leakage during the collection,
handling, processing, storage and transport of the
specimens. Any specimens which could puncture a
primary container are placed within a secondary
container which is puncture resistant.
If
outside contamination of the primary container
occurs, the primary container is placed within a
secondary container which prevents leakage during
the handling, processing, storage, transport or
shipping of the specimen.
7.
Contaminated
Equipment
. Equipment
which has become contaminated with blood
or
other potentially infectious materials is examined
prior to servicing or shipping and decontaminated as
necessary unless the decontamination of the
equipment is not feasible.
8.
Personal
Protective Equipment
. The
required personal protective equipment is
provided
to employees at no cost to them. Appropriate PPE in
a variety of sizes is readily accessible at the work
site or is issued to employees. Hypoallergenic
gloves, glove liners, powderless gloves, or other
similar alternatives are readily accessible to those
employees who are allergic to the gloves normally
provided.
Training
in the use of PPE is provided and covers the
appropriate PPE for the tasks or procedures
employees perform. Types of PPE available to
employees are as follows.

All
employees using PPE must observe the following
precautions:
•
Wash
hands immediately or as soon as feasible after
removal of gloves or other PPE.
•
Remove
PPE after it becomes contaminated and before leaving
the work area
•
Used
PPE may be disposed of in ________ (List
appropriate containers for storage, laundering,
decontamination or disposal).
•
Wear
appropriate gloves when it can be reasonably
anticipated that there may be hand contact with
blood or OPIM and when handling or touching
contaminated items or surfaces; replace gloves if
torn, punctured, contaminated, or if their ability
to function as a barrier is compromised.
•
Utility
gloves may be decontaminated for reuse if their
integrity is not compromised; discard utility gloves
if they show signs of cracking, peeling, tearing,
puncturing or deterioration.
•
Never
wash or decontaminate disposable gloves for reuse.
•
Wear
appropriate face and eye protection when splashes,
sprays, spatters or droplets of blood or OPIM pose a
hazard to the eye, nose, or mouth
•
Remove
immediately any garment contaminated by blood or
OPIM in such a way as to avoid contact with the
outer surface.
All
employees are expected to use the required personal
protective equipment (PPE). An employee who
temporarily and briefly declines to use PPE must
report to the immediate supervisor (i.e., it was the
employee's professional judgment that in the
specific instance its use would have prevented the
delivery of healthcare or posed an increased hazard
to the safety of the worker or co-worker).
When the employee makes this judgment, the
supervisor will investigate and document the circumstances
in order to determine whether changes can be
instituted to prevent such occurrences in the
future.
All
personal protective equipment is cleaned, laundered
and disposed of at no cost to employees.
All repairs and replacements are made at no
cost to employees.
All
garments which are penetrated by blood must be
removed immediately or as soon as feasible. All
personal protective equipment must be removed prior
to leaving the work area. The following protocol has
been developed so that equipment is left at the work
area and is not taken home.
Disposable
gloves used at this facility are not to be washed or
decontaminated for re-use and are to be replaced as
soon as practical when they become contaminated or
as soon as feasible if they are torn, punctured, or
when their ability to function as a barrier is
compromised. Utility gloves may be decontaminated
for re-use provided that the integrity of the glove
is not compromised. Utility gloves are discarded if
they are cracked, peeling, torn, punctured, or
exhibit other signs of deterioration or when their
ability to function as a barrier is compromised.
9.
Housekeeping.
This facility is cleaned and decontaminated
according to the following schedule (list area and
schedule):
|
Area
|
Schedule
|
Cleaner
|
|
Example:
Contaminated work surfaces
|
Example:
After completion of procedures; immediately,
or as soon as possible, after spills or OPIM;
at the end of the work shift
|
List
materials used, such as bleach solutions or
EPA registered germicides
|
|
Example:
Bins, pails, cans or similar receptacles
|
When
|
How
|
|
Example:
Broken glassware which may be contaminated is
picked up using mechanical means, such as a
brush and dust pan.
|
When
|
How
|
Reusable
sharps that are contaminated with blood or other
potentially infectious materials shall not be stored
or processed in a manner that requires employees to
reach by hand into the containers where these sharps
have been placed.
The
following contaminated articles will be laundered by
this facility:___________ or Laundering will be
performed by ___________at ___________time/location.
Laundry
contaminated with blood or other potentially
infectious materials are handled as little as
possible. The laundry is placed in appropriately
marked bags at the location where it was used. The
laundry will not be sorted or rinsed in the area of
use.
10.
Labels. The following labeling method(s) is
used at this facility.
|
Equipment
to be Labeled
|
Label
type (size, color, etc.)
|
|
Example:
specimens, contaminated laundry containers
used to store, transport or ship blood or OPIM)
|
Example:
red bag, biohazard label, etc.
|
|
Example:
refrigerators and freezers containing blood or
OPIM
|
|
|
Example:
regulated waste or contaminated equipment
brought into the facility
|
|
11.
Regulated
Waste Disposal.
Regulated waste is placed in containers which are
closeable, constructed to contain all contents and
prevent leakage, appropriately labeled or
color-coded and closed prior to removal to prevent
spillage or protrusion of contents during handling.
The
container is placed in a secondary container if
leakage of the primary container is possible.
The second container must be closeable,
constructed to contain all contents and prevent
leakage during handling, storage and transport, or
shipping. The
second container must be labeled or color coded to
identify its contents.
a.
Disposable
Sharps. All
contaminated sharps are discarded as soon as
feasible in sharps containers which are closeable,
puncture resistant, leak proof on sides and bottom
and labeled or color coded.
During
use, containers for contaminated sharps is easily
accessible to personnel and located as close as
possible to the immediate area where sharps are used
or can be reasonably anticipated to be found (e.g.,
laundries). Sharps
containers are located in (specify locations of
sharps containers) _____________________. The
containers are maintained upright throughout use and
replaced routinely and are not allowed to overfill.
When
moving containers of contaminated sharps from the
area of use, the containers are closed immediately
prior to removal or replacement to prevent spillage
or protrusion of contents during handling, storage,
transport or shipping.
Reusable containers are not to be opened,
emptied, or cleaned manually or in any other manner
which would expose employees to the risk of
percutaneous injury.
b.
Other Regulated Waste. Regulated waste other
than sharps is placed in appropriate containers.
These containers are located in (specify locations
of containers.) ________________________.
The
waste is to be labeled or color coded and closed
prior to removal to prevent spillage or protrusion
of contents during handling, storage, transport or
shipping.
C.
Hepatitis B Vaccine & Post-exposure Evaluation
& Follow-up.
The Hepatitis B vaccine and vaccination series are
made available to all employees who have
occupational exposure. Training is provided to
employees on Hepatitis B vaccinations. The training
addresses the safety, benefits, efficacy, methods of
administration and availability.
1.
Hepatitis
B Vaccination. The vaccine is offered after the
employee has received the training in occupational
exposure (see information and training) and within
10 working days of their initial assignment to work
involving the potential for occupational exposure to
blood or other potentially infectious materials
unless the employee has previously received the
complete Hepatitis B vaccination series, or antibody
testing has revealed that the employee is immune, or
the vaccine is contraindicated for medical reasons.
Participation
in a pre-screening program is not a prerequisite for
receiving Hepatitis B vaccination.
Employees
who decline the Hepatitis B vaccine will sign a
waiver which uses the wording in Appendix A of the
OSHA Standard (sample attached). Employees who
initially decline the vaccine but who later (while
still covered under the standard) wish to have it
may then have the vaccine provided at no cost.
______________________________
has responsibility for assuring that the vaccine is
offered, the waivers are signed, etc.
___________________ will administer the
vaccine.
If
a routine booster dose of Hepatitis B vaccine is
recommended by the U.S. Public Health Service at a
future date, such booster doses will be made
available.
2.
Post
Exposure Evaluation & Follow-Up. Post
exposure follow-up is provided to employees who have
had an exposure incident. The employee is given
appropriate counseling concerning precautions to
take during the period after the exposure incident.
The employee will also be given information on what
potential illnesses to be alert for and to report
any related experiences to appropriate personnel.
Employees
report exposure incidents to (list who has
responsibility to maintain records of exposure
incidents) who will review the circumstances of the
exposure incident to determine:
•
engineering
controls in use at the time
•
work
practices followed
•
a
description of the device being used (including type
and brand)
•
protective
equipment or clothing that was used at the time of
the exposure incident (gloves, eye shields, etc.)
•
location
of the incident
•
procedure
being performed when the incident occurred
•
employee’s
training
A
confidential medical evaluation and follow-up is
conducted by ______HCP. Following the initial first
aid (clean the wound, flush eyes or other mucous
membranes, etc.), the following activities are
performed.
•
Document
routes of exposure and the circumstances related to
the incident.
•
Identify
and document the source individual unless it can be
established that identification is infeasible or
prohibited by state or local law.
•
Unless
already know to be infected, obtain consent and make
arrangements to have the source individual tested as
soon as possible to determine HIV, HCV and HBV
infectivity; document that the source individual’s
test results were conveyed to the employee’s
health care provider.
•
Assure
that the exposed employee is provided with the
source individual’s test results and with
information about applicable disclosure laws and
regulations concerning the identify and infectious
status of the source individual.
Collection
and testing of blood for HBV and HIV serological
status will comply with the following:
•
The
exposed employee's blood shall be collected as soon
as feasible and tested after consent is obtained.
•
If
employee does not give consent for HIV serological
testing during collection of blood for baseline
testing, preserve the baseline blood sample for at
least 90 days to allow the employee to decide if the
blood should be tested for HIV serological status.
If the employee elects to have the baseline sample
tested during this waiting period, perform testing
as soon as feasible.
•
Employees
are offered post exposure prophylaxis in accordance
with the current recommendations of the U.S. Public
Health Service. These recommendations are currently
as follows: (these
recommendations may be listed as an appendix to the
plan)
D.
Interaction with Health Care Professionals
l.
Information
provided to the Healthcare Professional.
The healthcare professional responsible for the
employee's Hepatitis B vaccination is provided with
the following:
•
A copy
of 29 CFR 1910.1030.
Note: while the standard outlines the
confidentiality requirements of the health care
professional, it might be helpful for the employer
to remind that individual of these requirements.
•
A
written description of the exposed employee's duties
as they related to the exposure incident;
•
Written
documentation of the route of exposure and
circumstances under which exposure occurred;
•
Results
of the source individuals blood testing if
available;
•
All
medical records relevant to the appropriate
treatment of the employee including vaccination
status.
2.
Healthcare
Professional's Written Opinion. A written
opinion is obtained from the health care
professional who evaluates employees of this
facility. The
employee are provided with a copy of the written
opinion within 15 days of the completion of the
evaluation. Written
opinions are obtained in the following instances:
•
When
the employee is sent to obtain the Hepatitis B
vaccine.
•
Whenever
the employee is sent to a health care professional
following an exposure incident.
The
healthcare professionals written opinion for HBV
vaccination is limited to whether HBV vaccination is
indicated for an employee and if the employee has
received such vaccination.
The
healthcare professionals written opinion for post
exposure follow-up is limited to a statement that
the employee:
•
Has
been informed of the results of the evaluation, and
•
Has
been told about any medical conditions resulting
from exposure to blood or other potentially
infectious materials.
(Note that the written opinion to the
employer is not to reference any personal medical information.)
Note:
All other findings or diagnosis will remain
confidential and shall not be included in the
written report.
All
medical evaluations and procedures, the Hepatitis B
vaccine and vaccination series and post exposure
follow-up, including prophylaxis, and laboratory
test are available at no cost to employees. They are
made available to employees at a reasonable time and
place; performed by or under the supervision of a
licensed physician or other licensed healthcare
professional; and provided according to the
recommendations of the U.S. Public Health Service.
E.
Information and Training
All
employees who have occupational exposure to
bloodborne pathogens receive training conducted by
______________________ (attach a brief description
of their qualifications if necessary). Training
materials are available at ___________________.
Training
is provided at the time of initial assignment to
tasks where occupational exposure may occur, and
that it is repeated within twelve months of the
previous training. Training includes epidemiology,
symptoms and transmission of bloodborne pathogen
diseases. Employees have an opportunity for
interactive questions and answers with the person
conducting the training sessions. In addition, the
training program covers, at a minimum, the following
elements.
•
A copy
and explanation of the standard.
•
An
explanation of our ECP and how to obtain a copy.
•
An
explanation of methods to recognize tasks and other
activities that may involve exposure to blood and
OPIM, including what constitutes an exposure
incident.
•
An
explanation of the use and limitations of
engineering controls, work practices and personal
protective equipment.
•
An
explanation of the types, use, location, removal,
handling, decontamination and disposal of personal
protective equipment.
•
An
explanation of the basis of selection of personal
protective equipment.
•
Information
on the Hepatitis B vaccination, including efficacy,
safety, method of administration, benefits and that
it are offered free of charge.
•
Information
on the appropriate actions to take and persons to
contact in an emergency involving blood or other
potentially infectious materials.
•
An
explanation of the procedures to follow if an
exposure incident occurs, including the method of
reporting and medical follow-up.
•
Information
on the evaluation and follow-up required after an
employee exposure incident.
•
An
explanation of the signs, labels and color coding
systems required by the standard and used at this
facility.
All
employees will receive annual refresher training.
Note that this training is to be conducted within
one year of the employee's previous training.
Additional training shall be provided to employees
when there are any changes of tasks or procedures
affecting the employee's occupational exposure.
F.
Recordkeeping
1.
Medical
Records. Medical records are maintained for each
employee with occupational exposure. The Program
Administrator is responsible for maintaining medical
records. These confidential records are kept for at
least the duration of employment plus 30 years. The
records shall include the following:
•
The
name and social security number of the employee.
•
A copy
of the employee's HBV vaccination status, including
the dates of vaccination.
•
A copy
of all results of examinations, medical testing and
follow-up procedures.
•
A copy
of the information provided to the healthcare
professional, including a description of the
employee's duties as they related to the exposure
incident, and documentation of the routes of
exposure and circumstances of the exposure.
Medical
records are provided upon request to the employee or
to anyone having written consent of the employee
within 15 working days. Requests should be addressed
to the Program Administrator.
2.
Training
Records. Training records are completed for each
employee upon completion of training. These
documents are maintained for three years. The
following information shall be documented:
•
The
dates of the training sessions.
•
An
outline describing the material presented; the
contents or a summary of the training sessions.
•
The
names and qualifications of persons conducting the
training.
•
The
names and job titles of all persons attending the
training sessions.
Training
records are provided upon request to the employee or
the employee’s authorized representative within 15
working days. Requests should be addressed to the
Program Administrator.
3.
Sharps
Injury Log.
In addition to the 1904, recordkeeping requirements,
all percutaneous injuries from contaminated sharps
are also recorded on the Sharps Injury Log. All
incidences must include at least the date of the
injury; the type and brand of the device involved;
the department or work area where the incident
occurred; an explanation of how the incident
occurred.
The
log is reviewed at least annually as part of the
annual evaluation of the program and is maintained
for at least five years following the end of the
calendar year that they cover. If a copy is
requested by anyone, it must have any personal
identifiers removed from the report.
G.
Dates, Evaluation and Review
All
provisions required by this standard were
implemented by (insert date). The Program
Administrator is responsible for annually reviewing
this program and its effectiveness, and for updating
this program as needed.
Statement
of Declination of Hepatitis B vaccination
I
understand that due to my occupational exposure to
blood or other potentially infectious materials I
may be at risk of acquiring hepatitis B virus (HBV)
infection. I have been given the opportunity to be
vaccinated with hepatitis B vaccine, at no charge to
myself. However, I decline hepatitis B vaccination
at this time. I understand that by declining this
vaccine, I continue to be at risk of acquiring
hepatitis B, a serious disease. If in the future I
continue to have occupational exposure to blood or
other potentially infectious materials and I want to
be vaccinated with hepatitis B vaccine, I can
receive the vaccination series at no charge to me.
_________________________
Sample
Exposure Incident Report
Information
provided to Dr._____________________________
Employee
Name:
Date
of exposure incident:
Location
of exposure incident:
Route(s)
of exposure:
Results
of Source Individual’s tests if possible (unless
prohibited by law):
Description
of employee’s duties related to exposure incident:
Circumstances
under which exposure occurred:
Results
of previous blood tests:
Test(s) conducted:
Test date:
Results:
Attachments:
1.
Employee’s
medical records relevant to appropriate treatment,
including vaccination status.
2.
One copy
of OSHA Regulation, 1910.1030, Bloodborne Pathogens.
Sample
Training Outline
1.
Introduction.
Introduce
self and other presenters as applicable. Class is
designed as initial training for new employees and
to satisfy annual follow-up annual training.
2.
List
objectives of Training.
•
Describe
the primary diseases that the exposure control plan
covers
•
Explain
modes of transmission of HBV and HIV
•
Define
the term “Universal Precautions.”
•
Define
the terms “engineering controls” and “work
practice controls” and be familiar with those used
in the workplace.
•
List
personal protective equipment that may serve as
effective barriers to infectious fluids.
•
Describe
labeling, contaminated waste, and laundry
procedures.
•
Identify
the general requirements of OSHA Regulation
1910.1030, Bloodborne Pathogens.
3.
Program
Requirements.
Give an overview of basic exposure control plan
elements, and where employees can obtain a copy.
4.
HBV
and HIV. Discuss
epidemiology, symptoms, and modes of transmission of
HBV and HIV.
5.
Exposure
Determination. Through question/answer discussion, have students
determine those tasks that may result in an exposure
incident.
6.
Methods
of Compliance. Discuss exposure controls and work practice
controls. Have students give examples of each where
they work.
7.
Personal
Protective Equipment. Show a video, or present samples of various types of
personal protective equipment and how they form
effective barriers to infectious fluids. Demonstrate
proper wear, handling, decontamination, removal and
disposal.
8.
Post
Exposure Procedures. Explain specific emergency procedures if an exposure
incident occurs. Include notification, evaluation
and follow-up procedures.
9.
HBV
Vaccine Information. Explain
how effective and safe HBV vaccinations are, and the
benefits of being vaccinated. Emphasize that the
vaccinations are free to employees.
10.
Question
and Answer Period. Ensure an expert source is available to answer
questions employees may have regarding any part of
the exposure control plan or HBV/HIV disease.
11.
Conclusion.
Administer
and review post-training test with students. (Tests
need not be graded, but should serve as a tool to
determine if a review is necessary).
Establishment
Name
Year
200_
|
Date
|
Case/
Report No.
(from
300 Log)
|
Type
of Device
(e.g.,
syringe, suture needle)
|
Brand Name of Device
|
Work Area where injury
occurred (e.g., Geriatrics, Lab, patient room)
|
Brief description of how
the incident occurred (i.e., procedure being done, action being
performed - disposal, injection; body part
injured
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
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29
CFR 1910.1030, OSHA’s Bloodborne Pathogens Standard,
in paragraph (h)(5), requires an employer to establish
and maintain a Sharp Injury Log for recording all
percutaneous injuries in a facility occurring from
contaminated sharps. The purpose of the Log is to aid
in the evaluation of devices being used in healthcare
and other facilities and to identify problem devices
or procedures requiring additional attention or
review. This Log must be kept in addition to the
injury and illness log required by 29 CFR 1904. The
Sharps Injury Log should include all sharps injuries
occurring in a calendar year. The log must be retained
for five years following the end of the year to which
it relates. The Log must be kept in a anner that
preserves the confidentiality of the affected
employee.
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