# FDA recall Z-0706-2020

> **DeRoyal Industries Inc** · Class II · device recall initiated 2019-11-21.

## Product

DeRoyal KNEE BRACE, WARRIOR RECOVERY:  1) REF KB9000-01  2) REF 11-450A-00  3) REF 1150UTPP

## Reason for recall

The Warrior Recovery Knee Brace has the potential to come apart due to the hinge breaking.

## Distribution

Nationwide, Australia, India, Saudi Arabia

## Key facts

- **Recall number:** Z-0706-2020
- **Recalling firm:** DeRoyal Industries Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2019-11-21
- **Report date:** 2019-12-25

- **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-0706-2020

## Citation

> AI Analytics. FDA recall Z-0706-2020. Retrieved 2026-06-24 from https://api.ai-analytics.org/recall/Z-0706-2020. Source: US FDA. Licensed CC0.

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*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*
