Device recall
Z-0156-2016: Smith & Nephew MOSAICPLASTY DP- Disposable Harvesting System 4.5 mm, Sterile…
FDA device recall · Class II · Smith & Nephew, Inc., Endoscopy Div.
Key facts
| Recall number (Z-number) | Z-0156-2016 |
|---|---|
| Recall event | 72205 |
| Product | Smith & Nephew MOSAICPLASTY DP- Disposable Harvesting System 4.5 mm, Sterile Part Number: 7209235 Intended Use: For arthroscopic (knee and ankle) and open osteochondral grafting fix for osteochondral (cartilage) defects. |
| Product code | HWE |
| Recalling firm | Smith & Nephew, Inc., Endoscopy Div. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 23, 2021 |
| 510(k) numbers | K964215 |
| FEI number | 1219602 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database