[Recalled] FMS neXtra¿ 3.5mm Aggressive Cutter Shaver Blades; Product Code: 283315 Intended to provide controlled cutting, shaving, and abrading of tissue during orthopedic procedures. — Product is incorrectly labeled | FDA 2015-11-20
The product on this page is subject to an official recall. We summarise the regulator's findings and the recommended action.
Recall details
| Product | FMS neXtra¿ 3.5mm Aggressive Cutter Shaver Blades; Product Code: 283315 Intended to provide controlled cutting, shaving, and abrading of tissue during orthopedic procedures. |
|---|---|
| Brand / manufacturer | DePuy Mitek, Inc., a Johnson & Johnson Co. |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-0657-2016 |
| Country of notice | United States |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 20 November 2015 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: Product is incorrectly labeled. The blade configuration in the affected lots does not match the description on the label.
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 DePuy Mitek, Inc., a Johnson & Johnson Co.
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.