Hamilton Medical AG recalls IntelliCuff
- Recalling company
- Hamilton Medical AG
- Product
- IntelliCuff, Portable automatic cuff pressure controller REF: 951001
- Reason
- 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.
- Classification
- Class II – may cause temporary or medically reversible health consequences
- Recall date
- May 22, 2026
- Reported
- Jul 8, 2026
- Distribution
- Worldwide - US Nationwide distribution in the states of AZ, CA, CO, FL, GA, HI, IL, KY, MA, MI, ND, NE, NE, NY, OH, PA, PR, SD, TX, VA, WA, WI, WV, WY and the country of Canada.
- Status
- Ongoing
- Quantity
- 962 units
- Lot / codes
- GTIN: 07630002800839/ Lot # range: 00001 -19732
- Company location
- Domat/Ems, N/A
- Recall type
- Voluntary: Firm initiated
- Recall number
- Z-2625-2026
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number Z-2625-2026 in the FDA Enforcement Report. Also see FDA recall press releases.
If you use this product, check the lot, NDC or model number against the official notice and follow its instructions. Do not stop a prescribed medicine or remove a medical device without talking to your doctor or pharmacist. Report problems to FDA MedWatch. FoodRecallNow summarizes public FDA data and is not medical advice.