Belmont Instrument recalls Hyperthermia Pump Procedure Kit (Model 902-00045) due to potential crack in female connector causing fluid leaks during use. Affected units include specific lot numbers and dates.
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 their Hyperthermia Pump Procedure Kit (model 902-00045) because a crack in the female connector on the Heat Exchanger could cause fluid leaks during priming. This risk exists in specific lots produced on October 5 and November 8, 2024.
The female quick connector on the Heat Exchanger set may crack, leading to fluid leaks when the rapid infuser is primed. This could potentially cause contamination or improper treatment if fluid leaks during use.
Medical professionals using the Hyperthermia Pump Procedure Kit for treatments are most at risk. The recall affects specific lots produced on October 5 and November 8, 2024.
Check for model number 902-00045 on the Hyperthermia Pump Procedure Kit. Affected units were produced on October 5 and November 8, 2024, with lot numbers 20241005 and 20241108.
Inspect the female connector on the Heat Exchanger set for cracks before use.
The product may have a crack in the female connector that could cause fluid leaks during priming, so it should not be used until the recall is addressed.
Model number 902-00045 is affected, with specific lot numbers 20241005 and 20241108.
Check for model number 902-00045 and lot numbers 20241005 or 20241108 on the Hyperthermia Pump Procedure Kit.
We’ve drafted a message you can send Belmont Instrument to request your refund or repair — edit it as you like.
Subject: Recall Z-1674-2025 — Belmont Instrument Belmont Instrument Hello, I own a Belmont Instrument that is covered by recall Z-1674-2025 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.
