Z-2753-2018 Class II Terminated
FDA device recall Z-2753-2018 was initiated by Handicare Usa Inc on November 3, 2017 and is designated Class II. Reason for recall: Premature strap wear and breakage at maximum weight conditions (625 lbs.). The recall status is terminated (terminated July 10, 2020). Affected quantity: 4.
Recall Details
- Product Type
- Devices
- Report Date
- August 29, 2018
- Initiation Date
- November 3, 2017
- Termination Date
- July 10, 2020
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 4
Product Description
Handicare P600 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.).
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,
Code Information
Device Model; 303090 and 303093