# FDA recall Z-2069-2025

> **CORIN MEDICAL, LTD.** · Class II · device recall initiated 2025-05-23.

## Product

Apex Knee System. Model Numbers: KC-50090, KC-50097, KC-50110, KC-50117, KC-50130, KC-50135, KC-50137, KC-50150, KC-50155, KC-50157, KC-50170, KC-50175, KC-50177, KC-50190, KC-50197, KC-52104, KC-52554, KC-52574, KC-52774, KC-55223, KC-55243

## Reason for recall

Investigation has identified that the age of the nylon packaging material has caused a loss of integrity of some pouches.

## Distribution

US  Nationwide distribution in the states of CA, CO, FL, IL, OK, TX, UT.

## Key facts

- **Recall number:** Z-2069-2025
- **Recalling firm:** CORIN MEDICAL, LTD.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-05-23
- **Report date:** 2025-07-09

- **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-2069-2025

## Citation

> AI Analytics. FDA recall Z-2069-2025. Retrieved 2026-07-27 from https://api.ai-analytics.org/recall/Z-2069-2025. Source: US FDA. Licensed CC0.

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*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*