PlainRecalls
FDA Devices Moderate Class II Ongoing

Western Oxytote DTE Digital VIPR (head only) Model: MNDR-600

Reported: December 1, 2021 Initiated: October 16, 2021 #Z-0268-2022

Product Description

Western Oxytote DTE Digital VIPR (head only) Model: MNDR-600

Reason for Recall

VIPR (Valve Integrated Pressure Regulator) - battery rupture, causing the plastic VIPR shroud to break apart with emission of fumes and smoke

Details

Units Affected
4974 units
Distribution
CT, MD, MT, OH
Location
Westlake, OH

Frequently Asked Questions

What product was recalled?
Western Oxytote DTE Digital VIPR (head only) Model: MNDR-600. Recalled by Western/Scott Fetzer Company. Units affected: 4974 units.
Why was this product recalled?
VIPR (Valve Integrated Pressure Regulator) - battery rupture, causing the plastic VIPR shroud to break apart with emission of fumes and smoke
Which agency issued this recall?
This recall was issued by the FDA Devices on December 1, 2021. Severity: Moderate. Recall number: Z-0268-2022.