Z-0786-2022 Class II Terminated
FDA device recall Z-0786-2022 was initiated by Wright Medical Technology, Inc. on Feb 15, 2022 and is designated Class II. Reason for recall: An incorrect screw is packaged in the product, which contains a locking screw instead of a non-locking screw. The recall status is terminated (terminated Oct 5, 2022). Affected quantity: 1 package.
Recall Details
- Product Type
- Devices
- Report Date
- Mar 23, 2022
- Initiation Date
- Feb 15, 2022
- Termination Date
- Oct 5, 2022
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 1 package
Product Description
Wright Medical Technology, Inc. ORTHOLOC Non-Locking Screw 2mm x 8mm, REF 5201120008, non-sterile, a component of the ORTHOLOC 2.0/2.4 Plate System.
Reason for Recall
An incorrect screw is packaged in the product, which contains a locking screw instead of a non-locking screw.
Distribution Pattern
International distribution to the country of France.
Code Information
Lot #73967511638696
Source
- Dataset
- openFDA device recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for Z-0786-2022
- openFDA file date
- Nov 3, 2026
- Loaded by RegDataLab
- Nov 4, 2026