Device recall
Z-1524-2010: Ascension PyroCarbon PIP Total Joint - Trials; Ascension PIP, sizes 10P, 20P…
FDA device recall · Class II · Ascension Orthopedics, Inc
Key facts
| Recall number (Z-number) | Z-1524-2010 |
|---|---|
| Recall event | 55191 |
| Product | Ascension PyroCarbon PIP Total Joint - Trials; Ascension PIP, sizes 10P, 20P, 30P and 40P. Ascension Orthopedics, 8700 Cameron Road, Suite 100, Austin, Texas 78754; TEL: 512 836-5001. Intended as an accessory to the Ascension PyroCarbon PIP Total Joint used in finger joint implant procedures where… |
| Product code | NEG |
| Recalling firm | Ascension Orthopedics, Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 27, 2010 |
| 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