# FDA recall Z-2422-2018

> **Cayenne Medical Inc.** · Class II · device recall initiated 2013-07-11.

## Product

AperFix AM Femoral Implant, Model numbers CM-2409 (9mm x 24 mm) and CM-2410 (10 mm x 24 mm).  For orthopedic use in ligament reconstruction.

## Reason for recall

Potential for AperFix 24 mm implant breaking inside the drilled femoral socket.

## Distribution

US nationwide distribution.

## Key facts

- **Recall number:** Z-2422-2018
- **Recalling firm:** Cayenne Medical Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2013-07-11
- **Report date:** 2018-07-18
- **Termination date:** 2018-09-14

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Scottsdale, AZ, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2422-2018

## Citation

> AI Analytics. FDA recall Z-2422-2018. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-2422-2018. Source: US FDA. Licensed CC0.

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