Hamilton Medical recalls IntelliCuff portable blood pressure cuffs with REF 951001 due to potential "Cuff System Leakage" error causing continuous motor operation and pressure failure.
Due to reported complaints, the cuff device may alarm with a "Cuff System Leakage" error. As a result, the motor may pump continuously and fail to maintain the cuff pressure set by the user.
Hamilton Medical is recalling IntelliCuff portable blood pressure cuffs that may show a "Cuff System Leakage" error. This could cause the device to run continuously and fail to maintain proper blood pressure readings.
The device may display a "Cuff System Leakage" error, causing the motor to run continuously. This prevents the cuff from maintaining the pressure setting the user intended, potentially leading to inaccurate blood pressure readings.
Users of IntelliCuff portable blood pressure cuffs with REF 951001 are affected. People who rely on accurate blood pressure monitoring for health management are most at risk.
Check for IntelliCuff portable blood pressure cuffs with REF 951001. The product was sold with GTIN 07630002800839 and lot numbers from 00001 to 19732.
Look for a "Cuff System Leakage" error message on the device display.
Confirm the product has REF 951001 and was sold with GTIN 07630002800839 or lot numbers 00001-19732.
Hamilton Medical is recalling IntelliCuff devices due to reported complaints about the "Cuff System Leakage" error causing inaccurate blood pressure readings.
Check for the "Cuff System Leakage" error message. If you have the device with REF 951001, verify the product details and contact Hamilton Medical for further instructions.
The recall record does not specify a fix or remedy for this issue.
We’ve drafted a message you can send Hamilton Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-2625-2026 — Hamilton Medical Hamilton Medical Hello, I own a Hamilton Medical that is covered by recall Z-2625-2026 from Hamilton Medical. 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.
