BD Medical Voluntarily Recalls BD PosiFlush™ SF Saline Flush Syringe 10mL
On April 16, BD Medical announced a voluntary recall for multiple lots of BD PosiFlush™ SF (Sterile Field) Saline Flush Syringe 10 mL. Eleven lot numbers were affected. Hemophilia of Georgia and Beacon pharmacies dispensed items from six of the lot numbers, including:
- 9011582
- 9017875
- 9045702
- 9060999
- 9079716
- 9143529
The lot number can be found on the syringe and case label. A full list of lot numbers is provided below.
If you have a product affected by this recall, dispose of the product immediately. We will replace these items for our clients as quickly as possible. If we run out of sterile saline, we will temporarily replace the product with non-sterile saline. If you have questions about using non-sterile saline, please contact your outreach nurse or call HoG at 770-518-8272.
For those living in Georgia, your outreach nurse will contact you with more details. Florida clients will be contacted by your local Hemophilia Treatment Center.
The recall was made because BD Medical identified holes in the packaging, which impacts package integrity and potentially compromises a sterile field. While the sterility of the outer surface of the syringe may be compromised, the saline solution and the sterile path of the syringe are not impacted.
This recall affects products with the unique device identification number (UDI) 50382903065535 and catalog reference number 306553. BD distributed the affected recalled lots between Feb. 28, 2019, through March 2, 2020. This recall does not affect any other products or lots.
There have been no reports of adverse events, injuries or deaths related to this recall to date.
Lot Numbers in This Recall:
8353952
9011582
9017875
9024676
9045702
9060999
9079716
9127571
9143529
9156595
9163601