PlainRecalls
FDA Devices Moderate Class II Terminated

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.

Reported: September 2, 2015 Initiated: July 27, 2015 #Z-2467-2015

Product Description

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.

Reason for Recall

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.

Details

Recalling Firm
Sunrise Medical (US) LLC
Units Affected
64 total wheelchairs, both models.
Distribution
Worldwide Distribution - US (nationwide) and Internationally to Australia, Germany and Canada.
Location
Fresno, CA

Frequently Asked Questions

What product was recalled?
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.. Recalled by Sunrise Medical (US) LLC. Units affected: 64 total wheelchairs, both models..
Why was this product recalled?
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.
Which agency issued this recall?
This recall was issued by the FDA Devices on September 2, 2015. Severity: Moderate. Recall number: Z-2467-2015.