Reported Aug 29, 2018 · Terminated
Handicare C Series Patient Lift Product Usage: A device used to lift and transport a patient from one place to another.
Handicare USA Inc.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Handicare Usa Inc · 10888 Metro Ct · Maryland Heights, MO · 63043-2413
Is this the product you have?
- Handicare
- C Series Patient Lift Product UsageA device used to lift and transport a patient from one place to another
- Lot codes and dates
Device Model323100323102323117323118323120323137323149323150323215323225323237323240323400323417323450323600323602323700323750323840323851323917323117Vand 323150V
- Amount recalled
- 716
This recall covers 2 products
The agency filed one notice per product. You are reading one of them; the other one is below.
Where it was sold
Why it was recalled
Premature strap wear and breakage at maximum weight conditions (625 lbs.).
This product could cause temporary or reversible health problems — stop using it.
Want the full recall guide?
The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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