Device recall
Z-1946-2013: IsoGel AIR 84, Support Surface. Intended to assist in improving human patient…
FDA device recall · Class II · Stryker Medical Division of Stryker Corporation
Key facts
| Recall number (Z-number) | Z-1946-2013 |
|---|---|
| Recall event | 65337 |
| Product | IsoGel AIR 84, Support Surface. Intended to assist in improving human patient outcomes. |
| Product code | IOQ |
| Recalling firm | Stryker Medical Division of Stryker Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 11, 2014 |
| FEI number | 1831750 |
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