FDA Device recall Z-2244-2018
Farabeuf Clamp for 3.5mm Screws PRO, Catalog # 705463
- FDA Device
- Class II
- terminated
- Published 2018-06-27
On 2018-06-27 the FDA classified a Class II recall of Farabeuf Clamp for 3.5mm Screws PRO, Catalog # 705463 by Stryker, citing laser etching which indicates whether the device is in compression or distraction mode appears to be on the wrong side of the lever arm.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2244-2018 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2018-05-04 |
| Published | 2018-06-27 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Stryker |
| Distribution | AR, CA, ID, IL, MD, MI, NJ, NY, OK, SD, TX |
Product
Farabeuf Clamp for 3.5mm Screws PRO, Catalog # 705463
Reason
Laser etching which indicates whether the device is in compression or distraction mode appears to be on the wrong side of the lever arm
Identifiers
| code_info | Lot # 04857V |
|---|
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-2244-2018%22
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