RecallDepth

BD Q-Syte, Luer Access Split-Septum, 0.10 ml, REF 385100, Becton Dickinson Infusion Therapy Systems Inc.

Company
Becton Dickinson Medical Systems
Recall Initiated
October 19, 2009
Posted
February 2, 2010
Terminated
October 19, 2010
Recall Number
Z-0750-2010
Quantity
950,000 units
Firm Location
Sandy, UT

Reason for Recall

Manufacturing defect may allow air entry into a central venous catheter, possibly resulting in an air embolism.

Distribution

Nationwide distribution.

Lot / Code Info

Lot Numbers 8268863, 8269020, 8275798, 8308321, 8308323, 8309553, 8331937, 8331940, 8354558, 9007921, 9009643, 9009646, 9028838, 9035029, 99035032.

Root Cause

Process control

Action Taken

Consignees were notified by B-D Urgent Medical Device Recall letter on 10/28/2009 and asked to return all unused affected lots. For information, call the company at 800-453-4538, option 2, extension 2341. Another letter was sent to all affected customers on 02/08/2010 notifying them of the extension of the recall to include Nexiva products. A response card was included to be returned whether or not product was on hand. B-D issued a press release on Febriuary 8, 2010. It can be found on www.bd.com at http://www.bd.com/contentmanager/b_article.asp?Item_ID=24486&ContentType_ID=1&BusinessCode=20001&d=BD+Worldwide&s=&dTitle=&dc=&dcTitle=

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