Z-0036-2007

Medline Strider Maxi 3 Scooter; a three wheeled battery operated scooter; manufactured by KYMCO, Kaohsiung...

Name: Z-0036-2007 Medline Strider Maxi 3 Scooter; a three wheeled battery operated scooter; manufactured by KYMCO, Kaohsiung...
Creator: Medline Industries Inc
Published: 2006-07-20
License: https://open.fda.gov/license/

MEDLINE INDUSTRIES, LP - Northfield / initiated 2006-07-20 / Terminated

FDA source

Medline Industries Inc began a recall of Medline Strider Maxi 3 Scooter; a three wheeled battery operated scooter; manufactured by KYMCO, Kaohsiung, Taiwan for Medline Industries, Inc., One Medline... on 2006-07-20. The reason FDA records is "Under conditions of heavy use, signs of overheating of the main battery cables have been observed". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-0036-2007
Status: Terminated
Initiated: 2006-07-20
Posted: 2006-10-17
Terminated: 2009-09-02
Recalling firm: MEDLINE INDUSTRIES, LP - Northfield
Product: Medline Strider Maxi 3 Scooter; a three wheeled battery operated scooter; manufactured by KYMCO, Kaohsiung, Taiwan for Medline Industries, Inc., One Medline Place, Mundelein, IL 60060 USA; model MDS807600 - red and MDS807600B - blue
Product code: INI Vehicle, Motorized 3-Wheeled
Reason for recall: Under conditions of heavy use, signs of overheating of the main battery cables have been observed.
FDA root cause: Other
Action: Medline sent 'Voluntary Field Correction' letters dated 7/20/06 to the direct accounts on the same date, informing them that the Strider Maxi 3 and Maxi 4 scooters have main battery cables that may overheat under conditions of heavy use, and that Medline will provide an upgrade kit to replace the battery cables. 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). Follow-up letters were sent to the distributors and end-users on 10/31/06. The end users were informed of the problem with the scooters, and were requested to call Medline at 800-289-9793, press 1, then press 3 and ask to transfer to 4674 (8:00 AM to 5:00 PM CST) to have the scooter upgraded. The end users were requested to inform the service technician that hey have one of the affected Maxi Scooters, and provide him with their full name, phone number and street address, as well as the name, address and/or phone number of teh store where the Medline Scooter was purchased. Medline will arrange with the dealership or retail store to upgrade the scooter at no cost to the end user.
Quantity in commerce: 93 scooters
Distribution: Nationwide
Product codes and lots: model MDS807600 - red and model MDS807600B - blue, all serial numbers

Product code INI

K041054Class IIMedline Strider Maxi 3Medline Industries, Inc. / cleared 2004-05-25

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device recall database and the FDA enforcement reports, both ingested from openFDA. The recall record supplies the product, the reason and the product code; the enforcement report supplies the classification. The two datasets are exported by FDA on different days, and the date above is the older of the two, so nothing on this page is newer than it says.

MDM adds the root cause tag, derived from FDA’s own root cause text, and the cross-links to the product code, the clearances named on the record and MDM coverage. Where a recall has not been joined to an enforcement report, no classification is shown.

Data as of 2026-09-30, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)