Western Digital VIPR Medical Device Recalled for Battery Rupture Risk
Western/Scott Fetzer is recalling Digital VIPR devices (Model MNDR-600) due to battery rupture risk that could cause plastic shroud breakage and fume emission. The recall affects 4974 units distributed from May 2020 to August 2021.
- Product
- Western Oxytote DTE Digital VIPR (head only) Model: MNDR-600
- Category
- Medical Device
- Distribution
- 4 states