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

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  Reason
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  Affected products

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