RecallDepth

BD PosiFlush SF Saline Flush Syringe 0.9 Sodium Chloride Injection, USP 10 mL REF 306553. Intended to be used only for the flushing of indwelling vascular access devices.10 mL BD PosiFlush Normal Saline Flush Syringes are generally compatible for use with syringe pumps.

This recall has been terminated (originally issued September 22, 2014).

Company
Becton Dickinson & Company
Recall Initiated
July 22, 2014
Posted
September 22, 2014
Terminated
April 21, 2015
Recall Number
Z-2673-2014
Quantity
3,088,320 units
Firm Location
Franklin Lakes, NJ
Official Source
View on FDA website ↗

Reason for Recall

BD received some reports of open seals found on the BD Posiflush SF Flush Syringe 10 mL (Ref #306553).

Distribution

Nationwide Distribution.

Lot / Code Info

REF #306553  Lot numbers 3024261 - exp 12-2015  3046276 - exp 01-2016 4128353 - exp 04-2017

Root Cause

Packaging

Action Taken

BD sent recall letters/recall response cards dated 7/22/2014 via e-mail or UPS 2nd day mail. Customers are asked to examine their inventory and quarantine any affected product subject to recall. Customers should complete the Recall Response Card and fax it back to BD at 1-201-847-6990. Any questions can be directed to 1-888-237-2762 option 3.

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