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Terminated

Handicare C Series Patient Lift Product Usage: A device used to lift and transport a patient from one place to another.

FDA Recall Z-2752-2018 · Posted None

Recalling FirmHandicare Usa Inc
Recall StatusTerminated
Product CodeFNL
Date Initiated2017-11-03
Date Terminated2020-07-10
Product Quantity716

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.

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