[Recalled] Vitagel; indicated in surgical procedures (other than in neurosurgical and ophthalmic) as an adjunct to hemostasis when control of bleeding by ligature or conventional procedures is ineffective or impractical. — Several shipments
The product on this page is subject to an official recall. We summarise the regulator's findings and the recommended action.
Recall details
| Product | Vitagel; indicated in surgical procedures (other than in neurosurgical and ophthalmic) as an adjunct to hemostasis when control of bleeding by ligature or conventional procedures is ineffective or impractical. |
|---|---|
| Brand / manufacturer | Orthovita, Inc., dBA Stryker Orthobiologics. |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-1353-2015 |
| Country of notice | United States |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 26 February 2015 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: Several shipments of Vitagel product (a surgical hemostat) required to be stored at 2 -8 degrees Celsius (C) were not delivered to customers within the validated delivery time.
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 Orthovita, Inc., dBA Stryker Orthobiologics.
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.