Device recall
Z-2343-2010: Service parts for Crank Screw Assembly (PN1069-042-010S and 1069-042110S)…
FDA device recall · Class II · Stryker Medical Div. of Stryker Corporation
Key facts
| Recall number (Z-number) | Z-2343-2010 |
|---|---|
| Recall event | 54265 |
| Product | Service parts for Crank Screw Assembly (PN1069-042-010S and 1069-042110S) Stryker Medical 3800 E. Centre Ave Portage MI 49002. Intended use: Service parts are replacement parts for the eye surgery stretcher. |
| Product code | FNJ |
| Recalling firm | Stryker Medical Div. of Stryker Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 21, 2011 |
| FEI number | 1831750 |
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