[Recalled] GENESIS(R) II, POSTERIOR STABILIZED ARTICULAR INSERT, SIZE 1-2, 13 MM QTY: (1), REF 71420806, STERILE EO, Smith & Nephew, Inc. Memphis, TN 38116 USA Orthopedic — The Tyvek(TM) lid on one, or both, of the two trays that form a
This is an official product-safety recall record. Below are the verified details from the issuing authority, in plain language.
Recall details
| Product | GENESIS(R) II, POSTERIOR STABILIZED ARTICULAR INSERT, SIZE 1-2, 13 MM QTY: (1), REF 71420806, STERILE EO, Smith & Nephew, Inc. Memphis, TN 38116 USA Orthopedic |
|---|---|
| Brand / manufacturer | Smith & Nephew Inc |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-0444-2014 |
| Country of notice | United States |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 27 August 2013 |
| EAN / barcode | 71420806 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: The Tyvek(TM) lid on one, or both, of the two trays that form a double barrier around the insert may not have been adequately sealed.
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.