Device recall
Z-3041-2011: Amsco V-PRO 1 and Amsco V-PRO 1 Plus Low Temperature Sterilization Systems Model…
FDA device recall · Class II · Steris Corporation
Key facts
| Recall number (Z-number) | Z-3041-2011 |
|---|---|
| Recall event | 59520 |
| Product | Amsco V-PRO 1 and Amsco V-PRO 1 Plus Low Temperature Sterilization Systems Model #MLR, Serial # 033250701 - 031581115. The STERIS Amsco V-PRO and V-PRO 1 Plus Low Temperature Sterilizer are self-contained stand alone devices, using vaporized hydrogen peroxide as the sterilant. The sterilizer is… |
| Product code | MLR |
| Recalling firm | Steris Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 27, 2013 |
| 510(k) numbers | K062297, K083097 |
| 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