Z-0380-05

Victory Motorized Vehicle, 3 wheel Model SC1600

Name: Z-0380-05 Victory Motorized Vehicle, 3 wheel Model SC1600
Creator: Pride Mobility Product Corp
Published: 2004-07-01
License: https://open.fda.gov/license/

Pride Mobility Product Corporation / initiated 2004-07-01 / Terminated

FDA source

Pride Mobility Product Corp began a recall of Victory Motorized Vehicle, 3 wheel Model SC1600 on 2004-07-01. The reason FDA records is "intermittent operation". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-0380-05
Status: Terminated
Initiated: 2004-07-01
Posted: 2005-01-05
Terminated: 2008-02-12
Recalling firm: Pride Mobility Product Corporation
Product: Victory Motorized Vehicle, 3 wheel Model SC1600
Product code: INI Vehicle, Motorized 3-Wheeled
Reason for recall: intermittent operation
FDA root cause: Other
Action: The recalling firm issued a safety alert notification to all dealers/distributors dated 7/04.
Quantity in commerce: 17000 units
Distribution: The product was shipped to medical supply stores nationwide. There are five foreign accounts in Australia, Canada Great Britain, Italy, and Netherlands. There are twelve government accounts.
Product codes and lots: Model SC1600

Product code INI

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)