Device recall
Z-0181-2020: Sterile Co-Flex LF2 3" - Product Usage: Single Use secondary wound dressing or…
FDA device recall · Class II · Andover Healthcare Inc.
Key facts
| Recall number (Z-number) | Z-0181-2020 |
|---|---|
| Recall event | 83239 |
| Product | Sterile Co-Flex LF2 3" - Product Usage: Single Use secondary wound dressing or compression wrap |
| Product code | FQM |
| Recalling firm | Andover Healthcare Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 9, 2020 |
| FEI number | 1220799 |
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