Device recall
Z-2746-2011: Stryker Wire Caddy, Stryker Instruments Wire Caddy, REF 505-505, STERILE, QTY 1…
FDA device recall · Class II · Stryker Instruments Division of Stryker Corporation
Key facts
| Recall number (Z-number) | Z-2746-2011 |
|---|---|
| Recall event | 58907 |
| Product | Stryker Wire Caddy, Stryker Instruments Wire Caddy, REF 505-505, STERILE, QTY 1, MANUFACTURED FOR STRYKER INSTRUMENTS, KALAMAZOO, MI USA 49001 (269) 323-7700 (800) 253-3210. This device is intended for use in the storage and retrieval of guide wires up to 9.8 ft. in length and recommended for guide… |
| Product code | MDM |
| Recalling firm | Stryker Instruments Division of Stryker Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 3, 2011 |
| FEI number | 1811755 |
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