Recall Z-1462-06 ยท JKA Tubes, Vials, Systems, Serum Separators, Blood Collection
Becton Dickinson & Company
BD Vacutainer Luer Adapter; Catalog #367290 and #367300.
| 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 | 3,324,000 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
| K991088 | VACUTAINER BRAND MULTIPLE SAMPLE LUER ADAPTER, BLOOD COLLECTION SETS AND SAFETY-LOK BLOOD COLLECTION, SAFETY BLOOD COLLE Becton Dickinson Vacutainer Systems, May 28, 1999 |