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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