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

Recall Z-1020-2015 — Quickie Q7 Adult Rigid Wheelchair Model EIR4.

U.S. FDA — Device Enforcement · United States · 2014-12-19 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1020-2015
Date of alert
2014-12-19
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Sunrise Medical (US) LLC
Product category
device
Product type
Devices
Reported risk: There is the potential for the height adjustable handle to dislodge due to failing locking mechanisms on specific identified chairs.
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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