Recall Z-1496-2026 ยท FMF Syringe, Piston
Becton Dickinson & Company
10mL Non-Sterile BD Luer-Lok Tip Syringe Only. Catalog Number: 301029. 850 bulk non-sterile units per case.
| Date | Mar 6, 2026 (initiated Jan 27, 2026) |
| Status | Open, Classified |
| Reason | During the bulk packaging process, some Luer Slip syringes were incorrectly included in a batch designated for Luer Lok syringes. |
| Root cause | Under Investigation by firm |
| Action | Becton Dickinson notified consignees on about 01/27/2026 via emailed URGENT: Medical Device Recall (Correction) letter. Consignees were instructed to visually verify that the correct syringe is selected for the intended clinical application prior to use and that it forms a secure connection, destroy any luer slip syringes found in inventory, circulate the notification to all personnel who need to be aware or to any organization where the potentially affected products have been transferred, and complete and return the provided Customer Response Form. Distributors and kit manufactures were ins |
| Quantity | 204,000 units |
| Distribution | US Nationwide distribution in the states of California and Texas. |
| FDA record | Open on fda.gov |
510(k) clearances named in this recall
| K980987 | BECTON DICKINSON SYRINGE Bd Becton Dickinson Vacutainer Systems Preanalytic, Jun 11, 1998 |