Z-2244-2018 Class II Terminated
FDA device recall Z-2244-2018 was initiated by Stryker GmbH on May 4, 2018 and is designated Class II. 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 The recall status is terminated (terminated Apr 27, 2020). Affected quantity: 18 parts (10 parts quarantined).
Recall Details
- Product Type
- Devices
- Report Date
- Jun 27, 2018
- Initiation Date
- May 4, 2018
- Termination Date
- Apr 27, 2020
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 18 parts (10 parts quarantined)
Product Description
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
Distribution Pattern
AR, CA, ID, IL, MD, MI, NJ, NY, OK, SD & TX
Code Information
Lot # 04857V
Source
- Dataset
- openFDA device recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for Z-2244-2018
- openFDA file date
- Oct 23, 2026
- Loaded by RegDataLab
- Oct 26, 2026