Health product recall

BD Vacutainer Sodium Fluoride Tube (2019-06-14)

Starting date:
June 14, 2019
Posting date:
August 30, 2019
Type of communication:
Medical Device Recall
Subcategory:
Medical Device
Hazard classification:
Type II
Source of recall:
Health Canada
Issue:
Medical Devices
Audience:
General Public, Healthcare Professionals, Hospitals
Identification number:
RA-70849

Last updated: 2019-09-05

Affected Products

BD Vacutainer Sodium Fluoride Tube

Reason

BD is conducting a voluntary medical device recall for a lot of BD Vacutainer Fluoride Tubes for Blood Alcohol Determinations. A small portion of this lot has been confirmed to have no additive within tube.

Affected products

BD Vacutainer Sodium Fluoride Tube

Lot or serial number

8187663

Model or catalog number

367001

Companies
Manufacturer
Becton Dickinson and Company
1 Becton Drive
Franklin Lakes
07417
New Jersey
UNITED STATES