Device recall
Z-1561-2008: BD DifcoTM Neisseria Meningitidis Antisera Group Y 241113, 1mL, in vials, which…
FDA device recall · Class III · BD Diagnostic Systems / Lee Laboratories
Key facts
| Recall number (Z-number) | Z-1561-2008 |
|---|---|
| Recall event | 46750 |
| Product | BD DifcoTM Neisseria Meningitidis Antisera Group Y 241113, 1mL, in vials, which were labeled in part, 8019456 6250890 N. MEN. GP Y UNLABELED LYOPH, Becton, Dickinson and Company, Sparks, MD 21152. The product is packaged in 100 vial units For use in slide agglutination tests for serotyping Neisseria… |
| Product code | GTJ |
| Recalling firm | BD Diagnostic Systems / Lee Laboratories |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Mar 24, 2009 |
| 510(k) numbers | K844407 |
| FEI number | 1025402 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database