Sara Plus Active Floor Lift — Class I medical device recall Z-1098-2022
Terminated recall by ARJOHUNTLEIGH POLSKA Sp. z.o.o., reported 2022-06-01, distributed nationwide. The device may emit smoke or ignite.
| Recall number | Z-1098-2022 |
|---|---|
| Product type | Medical device |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | ARJOHUNTLEIGH POLSKA Sp. z.o.o., Komorniki, Poland |
| Recall initiated | 2022-04-05 |
| Classified | 2022-05-20 |
| Reported by FDA | 2022-06-01 |
| Terminated | 2024-09-05 |
| Distributed | Nationwide (US) |
| Quantity | 4,449 devices |
| Model numbers | HEP0001, HEP0001-AU, HEP0001-BR, HEP0001-CN, HEP0001-JP, HEP0001-UK, HEP0001-US, HEP1001, HEP1001-AU, HEP1001-US, HEP1001CON4869, HEP2001, HEP2001-BR, HEP2001-CN, HEP2001-UK |
Product
Sara Plus Active Floor Lift
Reason for recall
The device may emit smoke or ignite.
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-1098-2022. 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.