# FDA recall Z-1850-2021

> **Corin Ltd** · Class II · device recall initiated 2021-05-06.

## Product

Corin TriIFit TS SIZE 2, STANDARD TAPERED STEM, CEMENTLESS, REF 694.0002.  Hip prosthesis component.

## Reason for recall

Units from one batch of TriFit TS size 2 stem were found to be labeled as a TriFit CF size 7 stem. And vice versa.

## Distribution

US Nationwide distribution in the state of TX.

## Key facts

- **Recall number:** Z-1850-2021
- **Recalling firm:** Corin Ltd
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2021-05-06
- **Report date:** 2021-06-23
- **Termination date:** 2023-07-05

- **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-1850-2021

## Citation

> AI Analytics. FDA recall Z-1850-2021. Retrieved 2026-06-12 from https://api.ai-analytics.org/recall/Z-1850-2021. Source: US FDA. Licensed CC0.

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