Belmont Instrument LLC recalls 3.0L Disposable Sets (model 903-00032) due to potential cracks in the heat exchanger connector causing fluid leaks during priming. Affected units sold with lot numbers 20240911-20241105.
Potential crack in the female connector located on the Heat Exchanger/patient line set, which will lead to a fluid leak through the crack during priming of the Rapid Infuser.
Belmont Instrument recalls 3.0-liter disposable sets (model 903-00032) because the heat exchanger connector may crack during priming, leading to fluid leaks. This could cause contamination or equipment malfunction if not addressed.
The female quick connector on the heat exchanger/patient line set may crack during priming, creating a gap that allows fluid to leak. This could lead to contamination of the medical device or improper fluid delivery during use.
Users of the 3.0L Disposable Set (model 903-00032) with lot numbers 20240911 through 20241105 are affected. Healthcare professionals using this set for medical applications are most at risk.
Check for the model number 903-00032 on the packaging. The affected units were sold with lot numbers 20240911, 20241004, 20241011, or 20241105.
Verify the model number (903-00032) and lot numbers (20240911, 20241004, 20241011, 20241105) on the packaging.
The model number is 903-00032.
Lot numbers 20240911, 20241004, 20241011, and 20241105 are affected.
The recall states the female quick connector may crack during priming, but there's no specific visual indicator mentioned in the record.
We’ve drafted a message you can send Belmont Instrument to request your refund or repair — edit it as you like.
Subject: Recall Z-1678-2025 — Belmont Instrument Belmont Instrument Hello, I own a Belmont Instrument that is covered by recall Z-1678-2025 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.
