Z-1376-05

UltraLite Vehicles powered by Rascal Motorized Vehicles

Name: Z-1376-05 UltraLite Vehicles powered by Rascal Motorized Vehicles
Creator: Electric Mobility Corp
Published: 2005-05-05
License: https://open.fda.gov/license/

Electric Mobility / initiated 2005-05-05 / Terminated

FDA source

Electric Mobility Corp began a recall of UltraLite Vehicles powered by Rascal Motorized Vehicles on 2005-05-05. The reason FDA records is "The engager set screw may become loose. This problem may cause the potentiometer to become off-center thus affecting the end users stopping capabilities". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-1376-05
Status: Terminated
Initiated: 2005-05-05
Posted: 2005-08-17
Terminated: 2006-10-03
Recalling firm: Electric Mobility
Product: UltraLite Vehicles powered by Rascal Motorized Vehicles.
Product code: ITI Wheelchair, Powered
Reason for recall: The engager set screw may become loose. This problem may cause the potentiometer to become off-center thus affecting the end users stopping capabilities.
FDA root cause: Other
Action: The firm sent out letters to their customers on 4/20/2005. The firm's sales representatives were also notified on 4/20/2005.
Quantity in commerce: 788 units
Distribution: The firm sells the vehicles via direct sales to end customers and also to company owned inventory with sales representatives. The distribution is nationwide.
Product codes and lots: All units distributed under Model Number UL370.

Product code ITI

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)