Device recall
Z-0549-03: Ascension PIP, Prosthesis, finger, semi-constrained, pyrolytic carbon…
FDA device recall · Class III · Ascension Orthopedics, Inc
Key facts
| Recall number (Z-number) | Z-0549-03 |
|---|---|
| Recall event | 25056 |
| Product | Ascension PIP, Prosthesis, finger, semi-constrained, pyrolytic carbon, uncemented. The Ascension PIP received Humanitarian Device Exemption approval on March 22, 2002, under HDE number H010005 |
| Product code | --- |
| Recalling firm | Ascension Orthopedics, Inc |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Dec 3, 2003 |
| FEI number | 3002788818 |
At a glance
- None 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