Belmont Instrument recalls Straight Inflow/Bifurcated Outflow Line Kit (Model 902-00038) due to potential cracks in the female connector causing fluid leaks during priming. Affected units may leak during use with Hyperthermia Pump.
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.
Belmont Instrument is recalling a sterile, single-use line kit for hyperthermia pumps because a crack in the female connector could cause fluid leaks during priming. This poses a risk of improper treatment or contamination if the leak occurs.
The female connector on the Heat Exchanger set may crack during use, leading to fluid leaks when priming the rapid infuser. This could cause improper treatment delivery or contamination of the patient's system.
Patients using the Hyperthermia Pump with this specific line kit are most at risk. The recall affects medical devices used in certain cancer treatments.
Check for the model number 902-00038 on the kit packaging. The kit includes a 4.4 Liter Reservoir, Heat Exchanger set, and Straight Inflow/Bifurcated Outflow Patient Line. All components are packaged together in one case.
Verify the model number 902-00038 on the packaging and ensure all three components (reservoir, heat exchanger, and line) are present.
Yes, this kit is used with the Hyperthermia Pump.
A crack could cause fluid leaks during priming, potentially leading to improper treatment or contamination.
Look for the model number 902-00038 on the packaging. The kit includes a 4.4 Liter Reservoir, Heat Exchanger set, and Straight Inflow/Bifurcated Outflow Patient Line.
We’ve drafted a message you can send Belmont Instrument to request your refund or repair — edit it as you like.
Subject: Recall Z-1676-2025 — Belmont Instrument Belmont Instrument Hello, I own a Belmont Instrument that is covered by recall Z-1676-2025 from Belmont Instrument. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
