• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

Class 2 Device Recall Victory Motorized Vehicle

  • Print
  • Share
  • E-mail
-
Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 


New Search Back to Search Results
 Class 2 Device Recall Victory Motorized Vehiclesee related information
Date Initiated by FirmJuly 01, 2004
Date PostedJanuary 05, 2005
Recall Status1 Terminated 3 on February 12, 2008
Recall NumberZ-0381-05
Recall Event ID 29817
Product Classification Vehicle, Motorized 3-Wheeled - Product Code INI
ProductVictory Motorized Vehicle 4 wheels Model SC1700
Code Information Model number SC1700
Recalling Firm/
Manufacturer
Pride Mobility Product Corp
182 Susquehanna Avenue
Exeter PA 18643
For Additional Information ContactMichael Zablocky
570-655-5574 Ext. 1410
Manufacturer Reason
for Recall
intermittent operation
FDA Determined
Cause 2
Other
ActionThe recalling firm issued a safety alert notification to all dealers/distributors dated 7/04.
Quantity in Commerce17000 units
DistributionThe 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.
Total Product Life CycleTPLC Device Report

1 A record in this database is created when a firm initiates a correction or removal action. The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Learn more about medical device recalls.
2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall.
3 For details about termination of a recall see Code of Federal Regulations (CFR) Title 21 §7.55.
-
-