Product Wiki · Recalls · U.S. FDA — Device Enforcement

Universal Quick Adjust under the following labels: 1) Aluminum… — recall Z-2104-2016

U.S. FDA — Device Enforcement · United States · 2016-02-17 · Class II

As described by U.S. FDA — Device Enforcement: Universal Quick Adjust under the following labels: 1) Aluminum crutch, adult, 1 pair per case, 2) Aluminum crutch, tall adult, 1 pair per case Aid the user in walking while relieving weight from one foot or leg.

Compiled from an official source — the facts on this page are reproduced from the issuing authority’s own published notice, which is linked above. No AI-generated text appears on this page. How we use AI →
Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2104-2016
Date of alert
2016-02-17
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Medical Depot Inc.
Product category
device
Product type
Devices
Recall status
Terminated — the recall action is complete and the FDA has closed it
Initiated by
Voluntary: Firm initiated
Distribution
Nationwide Distribution
Reported risk: Tip crutch failure involving the bottom of the metal portion which comes in contact with ground
Primary source: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?start_search=1&

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

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