[Recalled] RENOVATION, RADIAL OSTEOTOME BLADE, SIZE 14, REF 71369314, STERILE R, QTY: (1) — The stability data does not support the product labeled with a 10-year shelf li… | FDA 2017-03-30
Authorities recorded a safety problem with this product. The details below come directly from the government recall notice.
Recall details
| Product | RENOVATION, RADIAL OSTEOTOME BLADE, SIZE 14, REF 71369314, STERILE R, QTY: (1) |
|---|---|
| Brand / manufacturer | Smith & Nephew, Inc. |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-1911-2017 |
| Country of notice | United States |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 30 March 2017 |
| EAN / barcode | 4500029102 |
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 →
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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.