Device recall
Z-1563-2016: 3M Steri-Vac Gas Sterilizer/Aerator, models 5XL and 8XL.
FDA device recall · Class II · 3M Company - Health Care Business
Key facts
| Recall number (Z-number) | Z-1563-2016 |
|---|---|
| Recall event | 73117 |
| Product | 3M Steri-Vac Gas Sterilizer/Aerator, models 5XL and 8XL. |
| Product code | FLF |
| Recalling firm | 3M Company - Health Care Business |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 25, 2016 |
| 510(k) numbers | K902036 |
| FEI number | 2110898 |
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