Recall Z-1334-2013— Becton Dickinson & Co.

Name: FDA recall Z-1334-2013
Creator: U.S. Food and Drug Administration
Published: 2013-03-11

Class II · Terminated

Class II FDA medical device recall by Becton Dickinson & Co., initiated 2013-03-11, terminated 2013-06-24. It names one FDA 510(k) clearance: K803025. Product: BBL(tm) CDC Anaerobe 5% Sheep Blood Agar. Used for culturing microorganisms.. Reason: Microbiological media may be contaminated with bacteria..

Recalling firm: Becton Dickinson & Co.
Classification: Class II
Status: Terminated
Initiated: 2013-03-11
Terminated: 2013-06-24
Firm location: Sparks, MD, United States

510(k) clearances named in this recall

1 on FDA's record

K803025 — CDC ANAEROBE BLOOD AGARBd Becton Dickinson Vacutainer Systems Preanalytic·cleared 1980-12-22

K-numbers as listed on FDA's Recall Enterprise System record for this event (openFDA device/recall k_numbers). The recall may also cover devices cleared under other submissions not named here.

Product description

BBL(tm) CDC Anaerobe 5% Sheep Blood Agar. Used for culturing microorganisms.

Reason for recall

Microbiological media may be contaminated with bacteria.

Data sourced from openFDA. This site is unofficial and independent of the FDA.