FDA Medical Device Recalls (openFDA)
Kinsman Enterprises Inc: Easi-Care Gait Belt Metal Buckle (54", 60", and 72" lengths)
- Recall number
- Z-0161-2022
- Recalling firm
- Kinsman Enterprises Inc
- Product
- Easi-Care Gait Belt Metal Buckle (54", 60", and 72" lengths)
- Status
- Terminated
- Initiated
- 2021-09-10
- Posted
- not on file
- Terminated
- 2025-08-27
- Reason
- The belt may fail at lower loads than the labeled 600lbs.
- Root cause
- Component change control
- Action
- The recalling firm sent recall notification via email beginning 09/23/2021. The scope of the recall includes all product (Items 80805, 80806, and 80807) shipped between May 17, 2021 and August 11, 2021. Customers are asked to immediately check stock and quarantine any impacted product. Impacted product is not to be used. Recalled devices must be returned to the recalling firm and will be replaced. A Verification Form should be completed and returned via email to recall@kinsmanenterprises.com. Distributors must promptly notify any potentially impacted customers to which they have further distributed product.
- Quantity
- 13,123 units
- Distribution
- Distribution in CA, FL, GA, IL, KY, MI, MS, NC, NH, NJ, NY, OH, TN, VA
- Lot, serial or model codes
- Kinsman Product Numbers: 80805 (54"), 80806 (60"), and 80807 (72") UPC codes: 873704007275, 873704006773, 873704007282
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- IKZ
- Firm FEI
- 1000570634
- Firm city
- W Frankfort
- Firm state
- IL
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28