Device recall
Z-0700-2016: Biosure Ratchet Driver, Product No: 72201888 For delivery and placement of…
FDA device recall · Class II · Smith & Nephew, Inc., Endoscopy Div.
Key facts
| Recall number (Z-number) | Z-0700-2016 |
|---|---|
| Recall event | 72908 |
| Product | Biosure Ratchet Driver, Product No: 72201888 For delivery and placement of orthopedic screws. Arthroscopic surgical instrument |
| Product code | NBH |
| Recalling firm | Smith & Nephew, Inc., Endoscopy Div. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 22, 2021 |
| FEI number | 1219602 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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