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

Recall Z-2695-2014 — Fuze Manual Tilt Wheelchair. Fuze T50, Fuze T20 and Fuze T50 Jr

U.S. FDA — Device Enforcement · Canada · 2012-06-12 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2695-2014
Date of alert
2012-06-12
Country / jurisdiction
Canada
Risk level
Class II
Risk type
recall
Brand
Pdg Product Design Group Inc
Product category
device
Product type
Devices
Reported risk: The hex bolt head might shear and cause the axle plate to detach from the lower frame of the wheelchair and could collapse the wheels while in use.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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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