Device recall
Z-1398-05: Custom Procedure Trays, containing various configurations of medical and…
FDA device recall · Class II · Avid Medical Inc
Key facts
| Recall number (Z-number) | Z-1398-05 |
|---|---|
| Recall event | 33335 |
| Product | Custom Procedure Trays, containing various configurations of medical and surgical devices, packed in plastic pouches, labeled in part ***Avid Medical, The custom procedure tray company Toano, Virginia 23168***Sterile~Disposable~Single Use Only***, and further identified by the following catalog… |
| Product code | LRO |
| Recalling firm | Avid Medical Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 8, 2006 |
| 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