# FDA recall Z-0682-2023

> **DeRoyal Industries Inc** · Class II · device recall initiated 2022-11-03.

## Product

DeRoyal SHOULDER ARTHOSCOPY PACK, REF 89-10240.03

## Reason for recall

XXX

## Distribution

US:  Tennessee, Texas, New York, Wisconsin, Florida, Virginia, Massachusetts, Arizona, Missouri, Connecticut, New Jersey, Pennsylvania, North Carolina, Louisiana, Michigan, Minnesota, Ohio, Indiana, Kansas, Illinois, Alabama, Georgia, Mississippi

## Key facts

- **Recall number:** Z-0682-2023
- **Recalling firm:** DeRoyal Industries Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2022-11-03
- **Report date:** 2022-12-21

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Powell, TN, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0682-2023

## Citation

> AI Analytics. FDA recall Z-0682-2023. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/Z-0682-2023. Source: US FDA. Licensed CC0.

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