# FDA recall Z-1315-2025

> **DePuy Mitek, Inc., a Johnson & Johnson Co.** · Class II · device recall initiated 2025-02-24.

## Product

COR Disposable Kit, 8 mm w/ Perpendicularity. Cartilage Transplant System.

## Reason for recall

Device is missing the pin in the graft loader component.

## Distribution

Domestic: Nationwide Distribution; Foreign: Austria, Belgium, Brazil, Switzerland, Chile, China, Colombia, Czech Republic, Germany, Spain, Finland, France, French Guyana, Greece, Israel, India, Italy, Japan, South Korea, Luxemburg, Mexico, Netherlands, Poland, Portugal & Singapore.

## Key facts

- **Recall number:** Z-1315-2025
- **Recalling firm:** DePuy Mitek, Inc., a Johnson & Johnson Co.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-02-24
- **Report date:** 2025-03-19

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Norwood, MA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1315-2025

## Citation

> AI Analytics. FDA recall Z-1315-2025. Retrieved 2026-07-31 from https://api.ai-analytics.org/recall/Z-1315-2025. Source: US FDA. Licensed CC0.

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