# FDA recall Z-1821-2022

> **Ossur Americas** · Class II · device recall initiated 2022-08-29.

## Product

OSSUR Power Knee REF PKA10003    OSSUR Power Knee REF PKA10003    OSSUR Power Knee REF PKA01001L    OSSUR Power Knee REF PKA01001T

## Reason for recall

Battery may dislodge from the Power Knee

## Distribution

U.S. Nationwide distribution in the states of AL, AR, AZ, CA, FL, GA, HI, IA, IL, IN, LA, MA, MD, MI, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OR, PA, SC, SD, TN, TX, VA, VT, WA and WI.

## Key facts

- **Recall number:** Z-1821-2022
- **Recalling firm:** Ossur Americas
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2022-08-29
- **Report date:** 2022-10-05

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Foothill Ranch, CA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1821-2022

## Citation

> AI Analytics. FDA recall Z-1821-2022. Retrieved 2026-07-26 from https://api.ai-analytics.org/recall/Z-1821-2022. Source: US FDA. Licensed CC0.

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