OSSUR Power Knee REF PKA10003 OSSUR Power Knee REF PKA10003 OSSUR… — Class II medical device recall Z-1821-2022
Ongoing recall by Ossur Americas, reported 2022-10-05, distributed nationwide. Battery may dislodge from the Power Knee
| Recall number | Z-1821-2022 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Ossur Americas, Foothill Ranch, CA, United States |
| Recall initiated | 2022-08-29 |
| Classified | 2022-09-28 |
| Reported by FDA | 2022-10-05 |
| Distributed | Nationwide (US) |
| Quantity | 190 devices |
| UPC / GTIN / UDI-DI | 05690967642822, 05690967642839, 05690967648381, 05690967648749 |
| Serial numbers | 05690967642839, 05690967648749, HF511028, HF511029, HF511036, HF511037, HF511038, HF511042, HF511046, HF511047, HF511050, HF511051, HF511054, HF511058, HF511059, HF511060, HF511061, HF511064, HF511065, HF511070, HF511071, HF511072, HF511073, HF511075, HF511076 and 206 more |
| Model numbers | PKA01001L, PKA01001T, PKA10003 |
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
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1821-2022. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.