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.