# FDA recall Z-0595-2020

> **Zimmer Biomet, Inc.** · Class II · device recall initiated 2019-10-25.

## Product

Biomet Orthopedics Intramedullary Bone Saw Cam Assembly  14MM-  Orthopedic manual surgical instrument  Item Number: 475665

## Reason for recall

Possible commingle of 13 MM and 14 MM  Intramedullary Bone Saw Cam Assembly -an Intramedullary Bone Saw Cam Assembly was labeled and etched as a 14 MM but measured as a 13 MM cam

## Distribution

Distribution to US states of CA, FL, IN, MN, MO, NY, and UT,  Australia, and New Zealand

## Key facts

- **Recall number:** Z-0595-2020
- **Recalling firm:** Zimmer Biomet, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2019-10-25
- **Report date:** 2019-12-11
- **Termination date:** 2020-04-30

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Warsaw, IN, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0595-2020

## Citation

> AI Analytics. FDA recall Z-0595-2020. Retrieved 2026-06-24 from https://api.ai-analytics.org/recall/Z-0595-2020. Source: US FDA. Licensed CC0.

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