Recall Z-1849-2014— Western / Scott Fetzer Company

Class II · Terminated

Class II FDA medical device recall by Western / Scott Fetzer Company, initiated 2014-04-07, terminated 2016-10-14. FDA's recall record names no specific 510(k) clearance for this event. Product: Model RG3000 and RG4000 Series Valve Integrated Pressure Regulator (VIPR). Reason: Separation events have occurred, including the VIPR separating from the Aluminum cylinder..

Recalling firm
Western / Scott Fetzer Company
Classification
Class II
Status
Terminated
Initiated
2014-04-07
Terminated
2016-10-14
Firm location
Westlake, OH, United States

Product description

Model RG3000 and RG4000 Series Valve Integrated Pressure Regulator (VIPR)

Reason for recall

Separation events have occurred, including the VIPR separating from the Aluminum cylinder.

Data sourced from openFDA. This site is unofficial and independent of the FDA.