Farabeuf Clamp for 3 — Class II medical device recall Z-2244-2018
Terminated recall by Stryker GmbH, reported 2018-06-27, distributed in AR, CA, ID, IL, MD, MI, NJ, NY…. Laser etching which indicates whether the device is in compression or distraction mode appears to be on the wr
| Recall number | Z-2244-2018 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Stryker GmbH, Selzach, N/A, Switzerland |
| Recall initiated | 2018-05-04 |
| Classified | 2018-06-15 |
| Reported by FDA | 2018-06-27 |
| Terminated | 2020-04-27 |
| Distributed | AR, CA, ID, IL, MD, MI, NJ, NY, OK, SD, TX |
| Lot numbers | 04857V |
| Model numbers | 705463 |
Product
Farabeuf Clamp for 3.5mm Screws PRO, Catalog # 705463
Reason for recall
Laser etching which indicates whether the device is in compression or distraction mode appears to be on the wrong side of the lever arm
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2244-2018. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.