Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-0270-2022 — Western Oxytote DTE Digital VIPR System (with E-size cylinder) Model: MNDS-603

U.S. FDA — Device Enforcement · United States · 2021-10-16 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0270-2022
Date of alert
2021-10-16
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Western/Scott Fetzer Company
Product category
device
Product type
Devices
Reported risk: VIPR (Valve Integrated Pressure Regulator) - battery rupture, causing the plastic VIPR shroud to break apart with emission of fumes and smoke
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.