Device recall
Z-0581-2018: AVID Medical QA Pack AV10654-10
FDA device recall · Class II · Avid Medical, Inc.
Key facts
| Recall number (Z-number) | Z-0581-2018 |
|---|---|
| Recall event | 79135 |
| Product | AVID Medical QA Pack AV10654-10 |
| Product code | LRO |
| Recalling firm | Avid Medical, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 17, 2018 |
| FEI number | 1047429 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1,000+ 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