[Recalled] RENOVATION, THIN OSTEOTOME BLADE, 10 MM X 3 INCH, REF 71369210, STERILE R, QTY: (1) — The stability data does not support the product labeled with a 10-year shelf li… | FDA 2017-03-30
Regulators flagged this product in an official safety action. Here is what the notice says and what it means for owners.
Recall details
| Product | RENOVATION, THIN OSTEOTOME BLADE, 10 MM X 3 INCH, REF 71369210, STERILE R, QTY: (1) |
|---|---|
| Brand / manufacturer | Smith & Nephew, Inc. |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-1914-2017 |
| Country of notice | United States |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 30 March 2017 |
| EAN / barcode | 11150707 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: The stability data does not support the product labeled with a 10-year shelf life.
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 Smith & Nephew, Inc.
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.