# FDA recall Z-0972-2019

> **Zimmer Biomet, Inc.** · Class II · device recall initiated 2018-12-21.

## Product

Comprehensive Reverse Shoulder System Glenosphere Mini Baseplate with Taper Adapter, Model Number 010000589     Biomet Comprehensive Reverse Shoulder products are indicated for use in patients whose shoulder joint has a grossly deficient rotator cuff with severe arthropathy and/or previously failed shoulder joint replacement with a grossly deficient rotator cuff.

## Reason for recall

The product was potentially being packaged without a taper adapter.

## Distribution

US Distribution to states of:: AR, KY, and WA.; Internationally  to: Australia and Japan.

## Key facts

- **Recall number:** Z-0972-2019
- **Recalling firm:** Zimmer Biomet, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2018-12-21
- **Report date:** 2019-03-13
- **Termination date:** 2020-05-06

- **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-0972-2019

## Citation

> AI Analytics. FDA recall Z-0972-2019. Retrieved 2026-06-03 from https://api.ai-analytics.org/recall/Z-0972-2019. Source: US FDA. Licensed CC0.

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