medical MODERATE Updated 2026-07-08

Hamilton Medical AG recalls IntelliCuff, Portable automatic cuff pressure controller RE

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Recalled Product

IntelliCuff, Portable automatic cuff pressure controller REF: 951001

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Hazard / Issue

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.

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: GTIN: 07630002800839/ Lot # range: 00001 -19732

✅ What Should You Do?

  1. 1Contact your healthcare provider immediately to discuss this recall.
  2. 2Stop using the device if it is safe to do so, and contact your provider.
  3. 3Follow the manufacturer's remedy instructions provided in the recall notice.
  4. 4Report device problems to FDA MedWatch or call 1-800-FDA-1088.

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