Class II — Handicare Usa Inc
| Recalling firm | Handicare USA, Inc. |
|---|---|
| Registered facility | Handicare USA, Inc. (the firm's only registered facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | Premature strap wear and breakage at maximum weight conditions (625 lbs.). |
| Product | Handicare P600 Series Patient Lift Product Usage: A device used to lift and transport a patient from one place to another. |
| Quantity | 4 |
| Distribution | Worldwide Distribution - US Nationwide in the states of AK, CA, CT, DE, GA, IA, IL, KY, LA, MA, ME, MI, MN, MO, NE, NV, NY, OH, OR, PA, RI, TN, TX, WI, and Puerto Rico and the countries of Canada and Australia, |
| Initiated | 2017-11-03 |
| Classified | 2018-08-20 |
| Terminated | 2020-07-10 |
| Recall number | Z-2753-2018 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Handicare Usa Inc (Z-2753-2018).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/80556/
Alerts for Handicare USA, Inc.
Watchlist alerts will email you when FDA publishes a new recall, inspection classification, or warning letter for a facility you follow. They aren't open to the public yet — leave your email and we'll tell you when they are.
Want a one-page facility brief?
A single-page summary of this facility's registration and recall history for diligence. Not selling it yet — register interest and we'll follow up.