---
title: "Wright Medical Technology, Inc. ORTHOLOC Non-Locking Screw 2mm x 8mm, REF 520... — FDA record Z-0786-2022 | Is It on Recall"
description: "An incorrect screw is packaged in the product, which contains a locking screw instead of a non-locking screw."
url: https://isitonrecall.com/recall/fda-device-z-0786-2022-wright-medical-technology-inc-ortholoc-non-locking-screw-2mm-x-8mm-ref-5201120008-non-sterile-a-comp/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / 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](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## 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

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0786-2022%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). 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.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0786-2022%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Wright Medical Technology Inc records](https://isitonrecall.com/brand/wright-medical-technology-inc/)