Medline Strider Midi 3 Scooter; a three wheeled battery operated scooter; manufactured by KYMCO, Kaohsiung, Taiwan for Medline Industries, Inc., One Medline Place, Mudelein, IL 60060 USA; model MDS807500 - red and MDS807500B - blue
FDA Recall Z-1522-06 · Posted 2006-09-23
Recalling FirmMedline Industries Inc
Recall StatusTerminated
Product CodeINI
Date Initiated2006-07-20
Date Terminated2009-09-02
Product Quantity269 scooters
Reason for Recall
The P&G Solo 60A electronic control unit on the Midi Scooters may overheat.
Firm Action
Medline sent 'Voluntary Field Correction' letters dated 7/20/06 to the direct accounts on the same date, informing them that the Strider Midi 3 and Midi 4 scooters have an older version of the electronic control unit that may overheat, which Medline will replace with a newer version of the controller. Any questions were directed to 800-289-9793, press 1, then press 3 and ask to transfer to 4674 (8:00 AM to 5:00 PM CST).
Root Cause
Other
Distribution Pattern
Nationwide
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.