Device recall
Z-1786-2021: FISTULA (ON/OFF) ALL IN ONE BAG. Medical convenience kit, Avid Medical Part…
FDA device recall · Class I · Avid Medical, Inc.
Key facts
| Recall number (Z-number) | Z-1786-2021 |
|---|---|
| Recall event | 87720 |
| Product | FISTULA (ON/OFF) ALL IN ONE BAG. Medical convenience kit, Avid Medical Part Number: VAMK024-03 |
| Product code | OEZ |
| Recalling firm | Avid Medical, Inc. |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Jul 18, 2022 |
| FEI number | 1047429 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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