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

Recall Z-2467-2015 — Quickie IRIS Wheelchair. model EIZ4-2 in combination with option code 183M02 - MONO Backrest system with Dynamic Backrest option. Provide mobility to persons limited to a sitting position.

U.S. FDA — Device Enforcement · United States · 2015-07-27 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2467-2015
Date of alert
2015-07-27
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Sunrise Medical (US) LLC
Product category
device
Product type
Devices
Reported risk: Quickie IRIS and Zippie IRIS tilt-in-space wheelchairs with MONO Backrest System with Dynamic Backrest may break over time resulting in a fall or injury to occupant.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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