FDA Device recall Z-0700-2016
Biosure Ratchet Driver, Product No: 72201888 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 Ratchet Driver, Product No: 72201888 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-0700-2016 |
| 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 Ratchet Driver, Product No: 72201888 For delivery and placement of orthopedic screws. Arthroscopic 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: 50410950 and 50407175 |
|---|
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-0700-2016%22
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