# FDA recall Z-1036-2023

> **Biomet, Inc.** · Class II · device recall initiated 2022-11-29.

## Product

OSS Modular Arthrodesis Nail, 7 Degree Collar Assembly with Locking Bolts-For use in the replacement of segmental defects of long bone, including midshaft replacement, and arthrodesis of the knee  Item Number: CP260602

## Reason for recall

Product missing the four small locking collar bolts resulting in extension of surgery to find a replacement

## Distribution

US Nationwide distribution in the states of CA, KY, FL.

## Key facts

- **Recall number:** Z-1036-2023
- **Recalling firm:** Biomet, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2022-11-29
- **Report date:** 2023-02-08

- **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-1036-2023

## Citation

> AI Analytics. FDA recall Z-1036-2023. Retrieved 2026-07-10 from https://api.ai-analytics.org/recall/Z-1036-2023. Source: US FDA. Licensed CC0.

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