Western Oxytote DTE Digital VIPR recall
Western Oxytote DTE Digital VIPR (head only) Model: MNDR-600
Why was Western Oxytote DTE Digital VIPR recalled?
VIPR (Valve Integrated Pressure Regulator) - battery rupture, causing the plastic VIPR shroud to break apart with emission of fumes and smoke
What should I do if I have this product?
The recall is ongoing. Follow the firm and FDA instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
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)
- Product
- Western Oxytote DTE Digital VIPR (head only) Model: MNDR-600
- Recalling firm
- Western/Scott Fetzer Company
- Quantity
- 4974 units
- Distribution
- CT, MD, MT, OH
- Recall date
- December 1, 2021
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)