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FDA (Device enforcement)Recalled 2025-03-31class ii

Belmont Instrument LLC: Hyperthermia Pump Procedure Kit. Model Number: 902-00045. Sterile, single-use, disposable set used with the Hyperthermia Pump. The Hyperthermia Procedure kit (P/N 902-00045) co

Hazard

Potential crack in the female connector located on the Heat Exchanger in the set, which will lead to a fluid leak through the crack during priming of the rapid infuser.

Details from the source

Reason for recall: Potential crack in the female connector located on the Heat Exchanger in the set, which will lead to a fluid leak through the crack during priming of the rapid infuser. Distribution: Worldwide - US Nationwide distribution in the states of AZ, CA, CO, CT, DC, IL, IN, KS, KY, MA, ME, MN, NC, ND, NJ, NM, OH, OR, PA, SC, TN, TX, VA, VT, WA, WI, WV and the countries of Canada, Hungary, Korea (the Republic of), Latvia, Malaysia. Quantity: 158 sets Lot/code info: Model Number: 902-00045. UDI-DI: 00896128002589. Lot Numbers: 20241005, 20241108

UPC codes

00896128002589

Source

Official record: FDA (Device enforcement)

Republished from the official source above; details can change — the source record controls.

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