# FDA recall Z-1667-2022

> **Corin Ltd** · Class II · device recall initiated 2022-07-12.

## Product

TaperFit Stem, Size 0, 38mm OFFSET, 12/14 Taper + 188.550 Centraliser, For Cemented Use, REF 588.3800.  Orthopedic hip implant component.

## Reason for recall

Some of the devices did not pass fatigue testing.

## Distribution

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

## Key facts

- **Recall number:** Z-1667-2022
- **Recalling firm:** Corin Ltd
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2022-07-12
- **Report date:** 2022-09-07
- **Termination date:** 2026-05-04

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Cirencester, United Kingdom

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1667-2022

## Citation

> AI Analytics. FDA recall Z-1667-2022. Retrieved 2026-06-09 from https://api.ai-analytics.org/recall/Z-1667-2022. Source: US FDA. Licensed CC0.

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