Z-0161-2022 Class II Terminated
FDA device recall Z-0161-2022 was initiated by Kinsman Enterprises Inc on September 10, 2021 and is designated Class II. Reason for recall: The belt may fail at lower loads than the labeled 600lbs. The recall status is terminated (terminated August 27, 2025). Affected quantity: 13,123 units.
Recall Details
- Product Type
- Devices
- Report Date
- October 27, 2021
- Initiation Date
- September 10, 2021
- Termination Date
- August 27, 2025
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 13,123 units
Product Description
Easi-Care Gait Belt Metal Buckle (54", 60", and 72" lengths)
Reason for Recall
The belt may fail at lower loads than the labeled 600lbs.
Distribution Pattern
Distribution in CA, FL, GA, IL, KY, MI, MS, NC, NH, NJ, NY, OH, TN, VA
Code Information
Kinsman Product Numbers: 80805 (54"), 80806 (60"), and 80807 (72") UPC codes: 873704007275, 873704006773, 873704007282