FDA Recalls Western Oxytote DTE Digital VIPR System Due to Battery Rupture Risk
Western/Scott Fetzer Company is recalling 40 units of the Oxytote DTE Digital VIPR System due to battery rupture risk. The device may emit fumes and smoke when the battery ruptures and plastic shroud breaks apart.
- Product
- Western Oxytote DTE Digital VIPR System (with D-size cylinder) Model: MNDS-602
- Category
- Medical Device
- Distribution
- 4 states