---
title: "TaperFit Stem, Size 0, 38mm OFFSET, 12/14 Taper + 188.550 Centraliser, For Ce... — FDA record Z-1667-2022 | Is It on Recall"
description: "Some of the devices did not pass fatigue testing."
url: https://isitonrecall.com/recall/fda-device-z-1667-2022-taperfit-stem-size-0-38mm-offset-12-14-taper-188-550-centraliser-for-cemented-use-ref-588-3800-ortho/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# TaperFit Stem, Size 0, 38mm OFFSET, 12/14 Taper + 188.550 Centraliser, For Cemented Use, REF 588.3800. Orthopedic hip... — FDA record Z-1667-2022

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 Jul 12, 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**: TaperFit Stem, Size 0, 38mm OFFSET, 12/14 Taper + 188.550 Centraliser, For Cemented Use, REF 588.3800. Orthopedic hip implant component.
- **Reason**: Some of the devices did not pass fatigue testing.
- **Classification**: Class II
- **Recalling firm**: Corin Ltd
- **Quantity**: 1
- **Agency-reported status**: Terminated
- **Source record identifier**: Z-1667-2022

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1667-2022%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 | Model #588.3800, Lot #494754; UDI 05055343871065 |

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

## Distribution

Distribution was made to NJ. There was no military/government distribution.

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

- [New Jersey](https://isitonrecall.com/state/new-jersey/)

## Dates in the source

- **Report date**: Sep 7, 2022
- **Recall initiation date**: Jul 12, 2022
- **Center classification date**: Aug 31, 2022
- **Termination date**: May 4, 2026

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-1667-2022%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Corin Ltd records](https://isitonrecall.com/brand/corin-ltd/)