Recall Z-1009-2012 ยท FMI Needle, Hypodermic, Single Lumen
Becton Dickinson & Company
BD 30G1/2" Precision Glide" Needle Needles are used for aspiration and injection of medications
| Date | Feb 13, 2012 (initiated Oct 8, 2011) |
| Status | Terminated |
| Reason | Becton Dickinson has identified clogged needles. |
| Root cause | Device Design |
| Action | Becton Dickinson sent Urgent Product Recall letters dated October 18, 2011 and October 17, 2011, to all affected customers. The letter identified the product, the problem, and the action to be taken by the customer. Customers were instructed to check their inventory to deterine if they have any of the affected product. If they have affected product customers should return the product to Beckton Dickinson. For any questions regarding this recall call 201-847-4344. |
| Quantity | 480,000 units |
| Distribution | Nationwide Distribution including IL and NJ |
| FDA record | Open on fda.gov |
510(k) clearances named in this recall
| K021475 | BD SINGLE LUMEN NEEDLE, SYRINGE AND BLOOD COLLECTION SET Bd, Jul 19, 2002 |