[Recalled] Smith & Nephew MOSAICPLASTY DP- Disposable Harvesting System 6.5 mm, Sterile Part Number: 7209236 Intended Use: For arthroscopic (knee and ankle) and open osteochondral grafting fix for osteochondral (cartilage) defects. — S
Authorities recorded a safety problem with this product. The details below come directly from the government recall notice.
Recall details
| Product | Smith & Nephew MOSAICPLASTY DP- Disposable Harvesting System 6.5 mm, Sterile Part Number: 7209236 Intended Use: For arthroscopic (knee and ankle) and open osteochondral grafting fix for osteochondral (cartilage) defects. |
|---|---|
| Brand / manufacturer | Smith & Nephew, Inc., Endoscopy Div. |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-0157-2016 |
| Country of notice | United States |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 10 September 2015 |
| EAN / barcode | 50182767 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: Sterility of device is compromised due to breach in the packaging
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., Endoscopy Div.
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.