Device recall
Z-0813-2018: Surgical punch; sealed pouches packed in punch shelf box Intended for use by…
FDA device recall · Class II · Alto Development Corp
Key facts
| Recall number (Z-number) | Z-0813-2018 |
|---|---|
| Recall event | 79274 |
| Product | Surgical punch; sealed pouches packed in punch shelf box Intended for use by trained surgeons to create circular cuts in soft tissue or openings in soft vessel walls during surgical procedures. |
| Product code | LRY |
| Recalling firm | Alto Development Corp |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 30, 2019 |
| FEI number | 2242056 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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