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Terminated

Quickie Groove Power Wheelchair with QC (non-expandable) electronics, Model number EIPW13.

FDA Recall Z-1532-2008 · Posted 2008-08-23

Recalling FirmSunrise Medical Inc
Recall StatusTerminated
Product CodeITI
Date Initiated2008-01-11
Date Terminated2009-11-16
Product Quantity141 units total

Reason for Recall

Product experiences a longer than expected stopping distance, which may cause injury to the user, objects, or the chair itself.

Firm Action

Initial phone contact began on January 11, 2008. Medical device correction letters were also sent to affected dealers.

Root Cause

Software design

Distribution Pattern

Product was distributed to 126 retailers nationwide throughout the USA, as well as Canada and Australia.

Related FDA 510(k) Records

Devices referenced by this recall via K-numbers.

K060531QUICKIE RHYTHM & GROOVE SERIES POWER WHEELCHAIRS W/QUICKIE DELPHI CONTROLSSunrise Medical · 2006-03-17

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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