FDA Device recall Z-0699-2016
Biosure Driver, Product No: 72201887 For delivery and placement of orthopedic screws
- FDA Device
- Class II
- terminated
- Published 2016-02-10
On 2016-02-10 the FDA classified a Class II recall of Biosure Driver, Product No: 72201887 For delivery and placement of orthopedic screws by Smith And Nephew Endoscopy Div, citing driver does not meet specification, oversized. Driver may not be able to be fully inserted into the screw, or screw may become stuck on the driver.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0699-2016 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2013-04-04 |
| Published | 2016-02-10 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Smith And Nephew Endoscopy Div |
| Distribution | AK, AL, CA, CO, FL, IL, IN, MI, NE, NJ, NY, OH, OK, PA, SC, TN, TX |
Product
Biosure Driver, Product No: 72201887 For delivery and placement of orthopedic screws. Orthopedic Manual Surgical Instrument
Reason
Driver does not meet specification, oversized. Driver may not be able to be fully inserted into the screw, or screw may become stuck on the driver.
Identifiers
| code_info | Lot Numbers: 50409038, 50404149, 50399964 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0699-2016%22
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