Device recall
Z-0782-2021: Greffe Aorte-LF (product info is in French); Model DYNJ31877F - Product Usage…
FDA device recall · Class II · Medline Industries Inc
Key facts
| Recall number (Z-number) | Z-0782-2021 |
|---|---|
| Recall event | 86826 |
| Product | Greffe Aorte-LF (product info is in French); Model DYNJ31877F - Product Usage: This is a type of convenience kit used in various surgeries including cardiac, abdominal, and neck surgeries. |
| Product code | LRO |
| Recalling firm | Medline Industries Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 26, 2021 |
| FEI number | 1417592 |
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