Z-0903-06

Rascal 600F and 600T scooters, unspecified power wheelchair

Name: Z-0903-06 Rascal 600F and 600T scooters, unspecified power wheelchair
Creator: Electric Mobility Corp
Published: 2006-04-17
License: https://open.fda.gov/license/

Electric Mobility / initiated 2006-04-17 / Terminated

FDA source

Electric Mobility Corp began a recall of Rascal 600F and 600T scooters, unspecified power wheelchair on 2006-04-17. The reason FDA records is "The four seat mast mounting screws can loosen, causing seat to wobble. The chair seat actuator and portions of the seat can malfunction and/or break. Firm is aware of problems with the seat and injuries sustained from...". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-0903-06
Status: Terminated
Initiated: 2006-04-17
Posted: 2006-05-24
Terminated: 2014-04-08
Recalling firm: Electric Mobility
Product: Rascal 600F and 600T scooters, unspecified power wheelchair.
Product code: ITI Wheelchair, Powered
Reason for recall: The four seat mast mounting screws can loosen, causing seat to wobble. The chair seat actuator and portions of the seat can malfunction and/or break. Firm is aware of problems with the seat and injuries sustained from the powered wheelchair/scooter seat malfunction. Firm has not initiated recall, claims it is a Warranty Advisory.
FDA root cause: Other
Action: At this point, the firm has committed to send out a Warranty advisory. No recall has been initiated.
Quantity in commerce: 12,220 chairs
Distribution: To customers nationwide.
Product codes and lots: Numerous serial numbers

Product code ITI

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)