Reported Dec 1, 2021 · Ongoing
Western Oxytote DTE Digital VIPR System (with E-size cylinder) Model: MNDS-603
Western/Scott Fetzer Company
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Western/Scott Fetzer Company · 875 Bassett Rd · Westlake, OH · 44145-1142
Is this the product you have?
- Western Oxytote DTE Digital VIPR
- System (with E-size cylinder) ModelMNDS-603
- Lot codes and dates
- Units distributed from 05/29/20 to 08/31/21. Digital VIPR units manufactured and distributed after 08/31/21 are outside the scope of this recall and will be recognized by a green and silver control knob sticker (green logo, silver background)
- Amount recalled
- 40 units
This recall covers 4 products
The agency filed one notice per product. You are reading one of them; the other 3 are below.
Where it was sold
Why it was recalled
VIPR (Valve Integrated Pressure Regulator) - battery rupture, causing the plastic VIPR shroud to break apart with emission of fumes and smoke
This product could cause temporary or reversible health problems — stop using it.
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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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