# FDA recall Z-2272-2021

> **Biomet, Inc.** · Class II · device recall initiated 2021-06-02.

## Product

Arcos Modular Revision Hip System High Offset Cone Prox Body, Size E, 70 MM	    Item Number: 11-301335

## Reason for recall

Arcos Proximal Cone Bodies could potentially exhibit chatter in the inner taper fretting corrosion  and device failure in vivo leading to surgical intervention

## Distribution

US Nationwide distribution.

## Key facts

- **Recall number:** Z-2272-2021
- **Recalling firm:** Biomet, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2021-06-02
- **Report date:** 2021-08-18
- **Termination date:** 2022-07-06

- **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-2272-2021

## Citation

> AI Analytics. FDA recall Z-2272-2021. Retrieved 2026-06-10 from https://api.ai-analytics.org/recall/Z-2272-2021. Source: US FDA. Licensed CC0.

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