[Recalled] 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. — Surgical punches are being re
The product on this page is subject to an official recall. We summarise the regulator's findings and the recommended action.
Recall details
| 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. |
|---|---|
| Brand / manufacturer | Alto Development Corp |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-0813-2018 |
| Country of notice | United States |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 23 October 2017 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: Surgical punches are being recalled due to potential packaging damage which may have occurred during transportation resulting in loss of sterility.
This Class II recall concerns device products distributed in United States and was recorded by FDA_DEVICE. Recalls in this category are published so that owners, retailers, and importers can identify affected units and act quickly.
What to do if you own this product
Check whether your unit is affected and follow the authority's guidance before further use.
Read the full official notice →
Related recalls from Alto Development Corp
This page indexes a public government recall notice for reference. We do not sell or verify this product; always confirm the current status on the authority's official site.