# FDA recall Z-0093-2021

> **Biomet, Inc.** · Class II · device recall initiated 2020-09-02.

## Product

Biomet Comprehensive Reverse Shoulder Glenosphere Mini Baseplate with Taper Adapter-Shoulder Prosthesis   item: 010000589 - Product Usage: intended to serve as the foundation for the reverse shoulder prosthesis head (glenosphere).

## Reason for recall

Product potentially being packaged without a taper adapter or baseplate. The package should contain one (1) baseplate and one (1) taper adapter, product may be packaged with two (2) baseplates and no (0) adapters or with no (0) baseplates and two (2) adapters

## Distribution

US Nationwide distribution including in the states of CO, MN, OH, WY.

## Key facts

- **Recall number:** Z-0093-2021
- **Recalling firm:** Biomet, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2020-09-02
- **Report date:** 2020-10-21
- **Termination date:** 2020-12-31

- **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-0093-2021

## Citation

> AI Analytics. FDA recall Z-0093-2021. Retrieved 2026-07-27 from https://api.ai-analytics.org/recall/Z-0093-2021. Source: US FDA. Licensed CC0.

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