Events

Recall of Device Recall Victory Motorized Vehicle

According to U.S. Food and Drug Administration, this recall involved a device in United States that was produced by Pride Mobility Product Corp.

What is this?

A correction or removal action taken by a manufacturer to address a problem with a medical device. Recalls occur when a medical device is defective, when it could be a risk to health, or when it is both defective and a risk to health.

Learn more about the data here
  • Type of Event
    Recall
  • Event ID
    29817
  • Event Risk Class
    Class 2
  • Event Number
    Z-0381-05
  • Event Initiated Date
    2004-07-01
  • Event Date Posted
    2005-01-05
  • Event Status
    Terminated
  • Event Country
    United States
  • Event Terminated Date
    2008-02-12
  • Event Source
    USFDA
  • Event Source URL
    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=34611
  • Notes / Alerts
    U.S. data is current through June 2018. All of the data comes from the U.S. Food and Drug Administration, except for the category Manufacturer Parent Company.
    The Parent Company was added by ICIJ.
    The parent company information is based on 2017 public records.
  • Extra notes in the data
    Vehicle, Motorized 3-Wheeled - Product Code INI
  • Reason
    Intermittent operation.
  • Action
    The recalling firm issued a safety alert notification to all dealers/distributors dated 7/04.

Device

Device Recall Victory Motorized Vehicle
  • Model / Serial
    Model number SC1700
  • Product Classification
    Physical Medicine Devices
  • Device Class
    2
  • Implanted device?
    No
  • 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 Description
    Victory Motorized Vehicle 4 wheels Model SC1700
  • Manufacturer
    Pride Mobility Product Corp

Manufacturer

Pride Mobility Product Corp
  • Manufacturer Address
    Pride Mobility Product Corp, 182 Susquehanna Avenue, Exeter PA 18643
  • Source
    USFDA