Handicare C Series Patient Lift Product Usage: A device recall
Handicare C Series Patient Lift Product Usage: A device used to lift and transport a patient from one place to another.
Why was Handicare C Series Patient Lift Product Usage: A device recalled?
Premature strap wear and breakage at maximum weight conditions (625 lbs.).
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Device Model; 323100, 323102, 323117, 323118, 323120, 323137, 323149, 323150, 323215, 323225, 323237, 323240, 323400, 323417, 323450, 323600, 323602, 323700, 323750, 323840, 323851, 323917, 323117V, and 323150V
- Product
- Handicare C Series Patient Lift Product Usage: A device used to lift and transport a patient from one place to another.
- Recalling firm
- Handicare Usa Inc
- Quantity
- 716
- 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,
- Recall date
- August 29, 2018
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)