Becton Dickinson & Company BD Posiflush Pre-Filled Normal Saline Syringes Catalog Number: 306547 Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
BD Posiflush Pre-Filled Normal Saline Syringes Catalog Number: 306547
Brand
Becton Dickinson & Company
Lot Codes / Batch Numbers
Lot Number: 9142881 UDI: 50382903065474
Products Sold
Lot Number: 9142881 UDI: 50382903065474
Becton Dickinson & Company is recalling BD Posiflush Pre-Filled Normal Saline Syringes Catalog Number: 306547 due to Limited number of syringes labeled Posiflush Experimental Product and Not for Human Use being mixed with standard BD Posiflush Pre-Filled Normal S. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Limited number of syringes labeled Posiflush Experimental Product and Not for Human Use being mixed with standard BD Posiflush Pre-Filled Normal Saline Syringes.
Recommended Action
Per FDA guidance
BD issued notifications to Customers via FedEx to Distributors, Pharmacies, and Consumers via Pharmacies on 10/14/19, advising of the problem, health risk and action to take: Immediately review your inventory for the specific Catalog and Lot number listed , discontinue use and destroy all product subject to the recall following your institutions process for destruction.2. Complete the Customer Recall Response Form. Questions or require further assistance, please contact 1-888-731-7973 between 8 AM and 5 PM ET Monday through Friday.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026