[Recalled] Advanta SST Grafts <6mm Intended for use in arterial vascular reconstruction, segmental bypass, and for arteriovenous vascular access. — Inner tray label may adhere to wall of outer tray which make it difficult to re… | FDA 2013
Authorities recorded a safety problem with this product. The details below come directly from the government recall notice.
Recall details
| Product | Advanta SST Grafts <6mm Intended for use in arterial vascular reconstruction, segmental bypass, and for arteriovenous vascular access. |
|---|---|
| Brand / manufacturer | Atrium Medical Corporation |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-2316-2013 |
| Country of notice | United States |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 12 July 2013 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: Inner tray label may adhere to wall of outer tray which make it difficult to remove the tray onto the sterile field
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 Atrium Medical Corporation
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.