Recall archive / FDA device enforcement
Wright Medical Technology, Inc. ORTHOLOC Non-Locking Screw 2mm x 8mm, REF 5201120008, non-sterile, a component of the... — FDA record Z-0786-2022
Reported terminated
Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.
Source date Feb 15, 2022. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.
Archive changed Oct 1, 2026. USDA FSIS records are unavailable; check FSIS directly. Source coverage and dates.
What the record says
- Product
- 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
- An incorrect screw is packaged in the product, which contains a locking screw instead of a non-locking screw.
- Classification
- Class II
- Recalling firm
- Wright Medical Technology, Inc.
- Quantity
- 1 package
- Agency-reported status
- Terminated
- Source record identifier
- Z-0786-2022
What the recall classes mean. Classification is an agency assessment, not individual medical advice.
Lot and product identifiers
| Label field | Details supplied by the agency |
|---|---|
| Lot, code or applicability | Lot #73967511638696 |
Match all identifying details in the current notice. A brand name alone is not enough.
Distribution
International distribution to the country of France.
No US distribution state could be established from this record. Check the official notice.
Dates in the source
- Report date
- Mar 23, 2022
- Recall initiation date
- Feb 15, 2022
- Center classification date
- Mar 15, 2022
- Termination date
- Oct 5, 2022
FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.