Recall Z-1488-2009 ยท FMF Syringe, Piston
Becton Dickinson & Company
BD 20 ml Syringe Luer-Lok Tip Sterile, Do not reuse; Catalog Number 309661.
| Date | Jun 24, 2009 (initiated Apr 30, 2009) |
| Status | Terminated |
| Reason | Potential for compromised sterility: Insufficient packaging seals. |
| Root cause | Nonconforming Material/Component |
| Action | Becton Dickinson sent Urgent Product Recall letters on April 30, 2009 to all direct customers. Questions are to be directed to BD Customer Service at 1-888-237-2762. Letters to customers of distributors went out on May 12, 2009. |
| Quantity | 201,600 units |
| Distribution | Nationwide Distribution. |
| FDA record | Open on fda.gov |
510(k) clearances named in this recall
This recall record lists no 510(k) number.