FDAJanuary 15, 2025device
Vaporizer Sevoflurane, Quik-Fil. Model Number: 6682285. Device is a component of Flow-i C20, Flow-i C30, Flow-i C40, Flow-c, Flow-e. For use during anesthesia.
Official recall recorded by the U.S. Food & Drug Administration.
The hazard
Sevoflurane used with the vaporizer may degrade to hydrogen fluoride, which could present a risk to patients or health care providers through inhalation and/or skin exposure. Potential harms include irritation of respiratory tract, which in worst case may lead to lung edema and/or severe hypocalcemia, blistering, superficial ulceration, and/or hypomagnesemia.
What to do
FDA enforcement status: Ongoing
Brands named
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UPCs
07325710001141
Recall history
Other federal recalls tied to the same brand — a factual pattern, straight from the source data.
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- CPSCPressure Washers Recalled Due to Serious Risk of Injury or Death from Shock and Electrocution Hazards; Imported by BAYOTAK USA2026-04-16
- CPSCJC Sales Recalls Lil' Buddies Pet Laser Toys Due to Risk of Serious Injury or Death from Battery Ingestion Hazard; Violates Mandatory Standard for Consumer Products with Button Cell Batteries2026-04-16
- CPSCHead USA Recalls Ski Boots Due to Risk of Serious Injury from Fall Hazard2026-04-09
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