Z-1849-2014 Class II Terminated
FDA device recall Z-1849-2014 was initiated by Western / Scott Fetzer Company on April 7, 2014 and is designated Class II. Reason for recall: Separation events have occurred, including the VIPR separating from the Aluminum cylinder. The recall status is terminated (terminated October 14, 2016). Affected quantity: 118,325 units.
Recall Details
- Product Type
- Devices
- Report Date
- July 2, 2014
- Initiation Date
- April 7, 2014
- Termination Date
- October 14, 2016
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 118,325 units
Product Description
Reason for Recall
Distribution Pattern
Worldwide Distribution-USA (nationwide) including Puerto Rico and the states of Alaska, Arkansas, Arizona, California, Colorado, Connecticut, Delaware, Florida, Georgia, Hawaii, Idaho, Illinois, Indiana, Kansas, Kentucky, Louisiana, Massachusetts, Maryland, Michigan, Minnesota, Missouri, Mississippi, Montana, North Carolina, North Dakota, Nebraska, New Hampshire, New Jersey, New Mexico, Nevada, New York, Ohio, Oklahoma, Oregon, Pennsylvania, Rhode Island, South Carolina, South Dakota, Tennessee, Texas, Utah, Virginia, Washington, Wisconsin, and West Virginia and the countries of Canada,China, Costa Rica, France, Honduras, India, Ireland, Italy, Japan, Korea (South), Malaysia, Panama, Spain and Taiwan.