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Terminated

Sunrise Medical Quickie Power Wheelchairs: Three models -Rhythm, Groove, and Zippy Z-Bop (with Quickie IQ Enhanced Displays)

FDA Recall Z-1163-2007 · Posted 2007-08-14

Recalling FirmSunrise Medical Inc
Recall StatusTerminated
Product CodeITI
Date Initiated2007-04-23
Date Terminated2008-03-25
Product Quantity229 Enhanced Display units (affecting 220 wheelchairs)

Reason for Recall

The wire harness connected to the display housing (Quickie IQ Enhanced Displays) may separate and cause sparks from a short circuit.

Firm Action

Firm contacted consignees by phone and mailed May 1, 2007, Urgent Medical Device notification letters.

Root Cause

Component design/selection

Distribution Pattern

Product was distributed Worldwide.

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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