---
title: "Wright Medical Technology Inc. CHARLOTTE MTP Hex Screw, Model #41122718, 2.7m... — FDA record Z-0401-2022 | Is It on Recall"
description: "Incorrect product is contained in the packaging."
url: https://isitonrecall.com/recall/fda-device-z-0401-2022-wright-medical-technology-inc-charlotte-mtp-hex-screw-model-41122718-2-7mm-x-18mm-a-component-of-the/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement

# Wright Medical Technology Inc. CHARLOTTE MTP Hex Screw, Model #41122718, 2.7mm x 18mm, a component of the CHARLOTTE L... — FDA record Z-0401-2022

Reported ongoing

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 Dec 3, 2021. 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. CHARLOTTE MTP Hex Screw, Model #41122718, 2.7mm x 18mm, a component of the CHARLOTTE Lisfranc Reconstruction System.
- **Reason**: Incorrect product is contained in the packaging.
- **Classification**: Class II
- **Recalling firm**: Wright Medical Technology, Inc.
- **Quantity**: 22 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-0401-2022

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0401-2022%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 numbers 02010697711582590 and 02010697711582591, GTIN 00840420108340. |

Match all identifying details in the current notice. A brand name alone is not enough.

## Distribution

Worldwide distribution - US Nationwide distribution in the states of AZ, IA, and SC. The countries of Australia, Canada, Chile, Spain, and United Kingdom.

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

- [Alaska](https://isitonrecall.com/state/alaska/)
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- [Wyoming](https://isitonrecall.com/state/wyoming/)

## Dates in the source

- **Report date**: Dec 29, 2021
- **Recall initiation date**: Dec 3, 2021
- **Center classification date**: Dec 20, 2021

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-0401-2022%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/)
