Exact FDA event identifier

Event 88760

1 recalled-product record grouped only because every row carries this exact official event ID.

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Event summary

Timeline bucket: September 10, 2021
Product types: Device
Classifications: Class II
Statuses: Terminated
Recalling firm wording: Kinsman Enterprises Inc

Dossier provenance

Source snapshots represented here

openFDA Device Enforcement Report-date coverage June 20, 2012–July 08, 2026 Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.
openFDA Device Recall event_date_initiated coverage June 01, 1997–June 30, 2026

Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.

How coverage and grouping work

Complete imported group

Every recalled product in this event

1 official enforcement rows

Product dates, classifications, firms, and source wording remain attached to their individual rows. Opening this dossier never hides products that did not match a prior timeline filter.

device · product 1 of 1

Easi-Care Gait Belt Metal Buckle (54", 60", and 72" lengths)

Z-0161-2022

Recall number: Z-0161-2022
Initiated: September 10, 2021
Classification: Class II
Status: Terminated
Recalling firm: Kinsman Enterprises Inc
Quantity: 13,123 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0

The belt may fail at lower loads than the labeled 600lbs.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Component change control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The belt may fail at lower loads than the labeled 600lbs.

Code information

Kinsman Product Numbers: 80805 (54"), 80806 (60"), and 80807 (72") UPC codes: 873704007275, 873704006773, 873704007282

Distribution pattern

Distribution in CA, FL, GA, IL, KY, MI, MS, NC, NH, NJ, NY, OH, TN, VA