Handicare P600 Series Patient Lift Product Usage: A device used to lift and transport a patient from one place to another.
FDA Recall Z-2753-2018 · Posted None
Recalling FirmHandicare Usa Inc
Recall StatusTerminated
Product CodeFNL
Date Initiated2017-11-03
Date Terminated2020-07-10
Product Quantity4
Reason for Recall
Premature strap wear and breakage at maximum weight conditions (625 lbs.).
Firm Action
HandiCare USA sent an Urgent notification letter dated November 3, 2017 to their customers. The letter identified the affected product, problem and actions to be taken. Customers were informed new units will be sent to replace the affected units identified at no charge. For questions contact your Customer Service
Root Cause
Nonconforming Material/Component
Distribution Pattern
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,
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.