Handicare P600 Series Patient Lift Product Usage: A device used to lift and transport a patient from one place to another.
Class I - DangerousWhat Should You Do?
- Check if you have this product: Device Model; 303090 and 303093
- Do not eat it: Even if it looks and smells fine, do not consume this product.
- Throw it away or return it: You can return the product to the store for a full refund.
- Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
- Report problems: Report any issues to the FDA's Safety Reporting Portal.
⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.
Recall Details
- Company:
- Handicare Usa Inc
- Reason for Recall:
- Premature strap wear and breakage at maximum weight conditions (625 lbs.).
- Classification:
- Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
- Status:
- terminated
Product Information
Full Description:
Handicare P600 Series Patient Lift Product Usage: A device used to lift and transport a patient from one place to another.
Product Codes/Lot Numbers:
Device Model; 303090 and 303093
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: Z-2753-2018
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Handicare C Series Patient Lift Product Usage: A device used to lift and transport a patient from one place to another.
Handicare Usa
Premature strap wear and breakage at maximum weight conditions (625 lbs.).
During internal cycle testing of A-Series lifts Handicare has found that the A-Series lift strap for lifts manufactured between April 25, 2017 and June 12, 2017 may wear prematurely at max load (625 lbs). We have identified the root cause as a supplied component that was not to specification. If the strap wears during use there is a potential risk for the person being supported by the lift to drop.
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