Recall Z-2752-2018— Handicare Usa Inc
Class II · Terminated
Class II FDA medical device recall by Handicare Usa Inc, initiated 2017-11-03, terminated 2020-07-10. FDA's recall record names no specific 510(k) clearance for this event. Product: Handicare C Series Patient Lift Product Usage: A device used to lift and transport a patient from one place to another.. Reason: Premature strap wear and breakage at maximum weight conditions (625 lbs.)..
- Recalling firm
- Handicare Usa Inc
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2017-11-03
- Terminated
- 2020-07-10
- Firm location
- Maryland Heights, MO, United States
Product description
Handicare C 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.).
Data sourced from openFDA. This site is unofficial and independent of the FDA.