Device recall
Z-2238-2017: Non-Rebreather, Oxygen Mask, Adult 7 (2.1 m) Tubing, Product Code 3108-E…
FDA device recall · Class II · ConvaTec, Inc
Key facts
| Recall number (Z-number) | Z-2238-2017 |
|---|---|
| Recall event | 77282 |
| Product | Non-Rebreather, Oxygen Mask, Adult 7 (2.1 m) Tubing, Product Code 3108-E, Product Code 3108MM, Product Code 86-106E, Product Code 86-108-E, Product Code LM-86-106, Product Code PMD06002, Product Code PMD06003 |
| Product code | BYG |
| Recalling firm | ConvaTec, Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 27, 2021 |
| FEI number | 3011987967 |
At a glance
- None Linked 510(k)s
- 10–99 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