Handicare P600 Series Patient Lift Product Usage: A device used to… — Class II medical device recall Z-2753-2018
Terminated recall by Handicare Usa Inc, reported 2018-08-29, distributed nationwide. Premature strap wear and breakage at maximum weight conditions (625 lbs.).
| Recall number | Z-2753-2018 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Handicare Usa Inc, Maryland Heights, MO, United States |
| Recall initiated | 2017-11-03 |
| Classified | 2018-08-20 |
| Reported by FDA | 2018-08-29 |
| Terminated | 2020-07-10 |
| Distributed | Nationwide (US) |
| Countries outside the US | AU, CA |
| Quantity | 4 |
| Reason classes | device malfunction |
| Model numbers | 303090, 303093 |
Product
Handicare P600 Series Patient Lift Product Usage: A device used to lift and transport a patient from one place to another.
Reason for recall
Premature strap wear and breakage at maximum weight conditions (625 lbs.).
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-2753-2018. 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.