Class II — Stryker GmbH
| Recalling firm | STRYKER CORP. |
|---|---|
| Registered facility | View this company's 61 registered facilities → (openFDA recall records do not name a specific facility) |
| Classification | Class II |
| Status | Terminated |
| 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 |
| Product | Farabeuf Clamp for 3.5mm Screws PRO, Catalog # 705463 |
| Quantity | 18 parts (10 parts quarantined) |
| Distribution | AR, CA, ID, IL, MD, MI, NJ, NY, OK, SD & TX |
| Initiated | 2018-05-04 |
| Classified | 2018-06-15 |
| Terminated | 2020-04-27 |
| Recall number | Z-2244-2018 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Stryker GmbH (Z-2244-2018).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/80198/
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