Device recall
Z-0603-2016: AMSCO Warming Cabinet. Manufactured by: STERIS Corporation To raise the…
FDA device recall · Class II · Steris Corporation
Key facts
| Recall number (Z-number) | Z-0603-2016 |
|---|---|
| Recall event | 72825 |
| Product | AMSCO Warming Cabinet. Manufactured by: STERIS Corporation To raise the temperature of blankets, linens and sterile surgical IV/irrigation solutions to an acceptable level for various surgical, obstetrical, emergency, critical care and other healthcare applications. |
| Product code | LGZ |
| Recalling firm | Steris Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 27, 2016 |
| 510(k) numbers | K111870 |
| FEI number | 1527821 |
At a glance
- 1–9 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