Z-0910-03

Chauffeur Powered Scooters

Name: Z-0910-03 Chauffeur Powered Scooters
Creator: Electric Mobility Corp
Published: 2003-02-07
License: https://open.fda.gov/license/

Electric Mobility / initiated 2003-02-07 / Terminated

FDA source

Electric Mobility Corp began a recall of Chauffeur Powered Scooters on 2003-02-07. The reason FDA records is "The plastic tires may shatter if the tire is over-inflated and could cause serious injury". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-0910-03
Status: Terminated
Initiated: 2003-02-07
Posted: 2003-06-05
Terminated: 2008-03-03
Recalling firm: Electric Mobility
Product: Chauffeur Powered Scooters.
Product code: INI Vehicle, Motorized 3-Wheeled
Reason for recall: The plastic tires may shatter if the tire is over-inflated and could cause serious injury.
FDA root cause: Other
Action: All consignees were notified via personalized recall letter on 2/7/2003. The firm also posted the notice on their website on 2/14/2003. Customers will be asked to send back order form for new metal wheel tires.
Quantity in commerce: 45679
Distribution: Distribution is both nationwide and international. The distribution are to retail customers, intercompany sales, and dealers. The Veterans Administration, Canada, United Kingdom.
Product codes and lots: Chauffeur Model Numbers are C205, C215, C235, C245, C255, and C305. There are 45,679 serial numbers involved.

Product code INI

K924515Class IIElectric Mobility RascalElectric Mobility, LLC / cleared 1994-03-28

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)