Device recall
Z-1374-05: Coagulation Factor VIII Deficient Plasma (OTXW). Factor Deficiency Test
FDA device recall · Class III · Dade Behring, Inc.
Key facts
| Recall number (Z-number) | Z-1374-05 |
|---|---|
| Recall event | 32691 |
| Product | Coagulation Factor VIII Deficient Plasma (OTXW). Factor Deficiency Test |
| Product code | GJT |
| Recalling firm | Dade Behring , Inc. |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Aug 10, 2006 |
| 510(k) numbers | K924396 |
| FEI number | 2517506 |
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