Z-2069-2015 Class I Terminated
FDA device recall Z-2069-2015 was initiated by Western / Scott Fetzer Company on January 31, 2015 and is designated Class I. Reason for recall: The firm has become aware of the possibility of ignition and rupture (explosion) of a compressed gas oxygen cylinder, which can cause serious injury and/or death. The recall status is terminated (terminated January 18, 2018). Affected quantity: 162,678 units.
Recall Details
- Product Type
- Devices
- Report Date
- July 29, 2015
- Initiation Date
- January 31, 2015
- Termination Date
- January 18, 2018
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 162,678 units
Product Description
Reason for Recall
Distribution Pattern
Worldwide Distribution -- US, including the states of Alabama, Arkansas, Arizona, California, Colorado, Connecticut, Delaware, Florida, Georgia, Iowa, Idaho, Illinois, Indiana, Kansas, Kentucky, Louisiana, Massachusetts, Maryland, Maine, 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, West Virginia, and Wyoming; and, the countries of CANADA, CHILE, GERMANY, ISRAEL, LEBANON, MACAU, MEXICO, PUERTO RICO, and SINGAPORE.