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Terminated

Medline Strider Midi 4 Scooter; a four wheeled battery operated scooter; manufactured by KYMCO, Kaohsiung, Taiwan for Medline Industries, Inc., One Medline Place, Mudelein, IL 60060 USA; model MDS807550 - red and MDS807550B - blue

FDA Recall Z-1523-06 · Posted 2006-09-23

Recalling FirmMedline Industries Inc
Recall StatusTerminated
Product CodeINI
Date Initiated2006-07-20
Date Terminated2009-09-02
Product Quantity170 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Midi 4 scooters have an older version of the electronic control unit that may overheat, which Medline will replace with a newer version of the controller.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.

K042764MEDLINE STRIDER MIDI 4Medline Industries, Inc. · 2004-10-08

Official Source

View FDA Recall →

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

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