Recall Z-1461-06 ยท FMI Needle, Hypodermic, Single Lumen
Becton Dickinson & Company
BD Vacutainer Blood Collection Assembly with BD Blunt Plastic Cannula; Catalog #303380.
| Date | Sep 9, 2006 (initiated Jun 21, 2006) |
| Status | Terminated |
| Reason | Firm received complaints indicating failure of the Non-Patient (NP) sleeve to function properly. This sleeve covers the cannula and prevents leakage during blood collection. |
| Root cause | Other |
| Action | BD sent out recall notifications on 6/21/2006 to distributors and their direct account customers. |
| Quantity | 122,7900 units |
| Distribution | World wide-Products are distributed nationwide to distributors and direct accounts. The products are also distributed internationally to the following locations: Japan, Australia, Canada, Hong Kong, New Zealand. For European distribution, the products are shipped to Temse located in Belgium who ha |
| FDA record | Open on fda.gov |
510(k) clearances named in this recall
| K974363 | BECTON DICKINSON BLUNT PLASTIC CANNULA Bd Becton Dickinson Vacutainer Systems Preanalytic, Jun 3, 1998 |