Recall Z-1747-2015— Becton Dickinson & Co.

Name: FDA recall Z-1747-2015
Creator: U.S. Food and Drug Administration
Published: 2014-11-21

Class II · Terminated

Class II FDA medical device recall by Becton Dickinson & Co., initiated 2014-11-21, terminated 2016-01-07. FDA's recall record names no specific 510(k) clearance for this event. Product: BBL Port A Cul tubes with Swabs Sterile Pack, catalog number 221607. For patient sample collection.. Reason: The products may exhibit indications of excessive oxidation. Excessive oxidation may affect the viability of anaerobic microorganisms..

Recalling firm: Becton Dickinson & Co.
Classification: Class II
Status: Terminated
Initiated: 2014-11-21
Terminated: 2016-01-07
Firm location: Sparks, MD, United States

Product description

BBL Port A Cul tubes with Swabs Sterile Pack, catalog number 221607. For patient sample collection.

Reason for recall

The products may exhibit indications of excessive oxidation. Excessive oxidation may affect the viability of anaerobic microorganisms.

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