Device recall
Z-0619-2011: Inter-Op Acetabular System Hooded Trial Insert size 32mm/57mm, non-sterile, REF…
FDA device recall · Class II · Zimmer Inc.
Key facts
| Recall number (Z-number) | Z-0619-2011 |
|---|---|
| Recall event | 57304 |
| Product | Inter-Op Acetabular System Hooded Trial Insert size 32mm/57mm, non-sterile, REF 9363-32-057, Zimmer, Warsaw, IN. |
| Product code | HWT |
| Recalling firm | Zimmer Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 23, 2011 |
| FEI number | 1000220733 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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