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Medical Device

IntelliCuff, Portable automatic cuff pressure controller REF: 951001

Recall date: 2026-07-08 · Source: FDA_DEVICE
Brand / Firm
Hamilton Medical AG
Product
IntelliCuff, Portable automatic cuff pressure controller REF: 951001
Reason for recall
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.
Units affected
962 units
Description
IntelliCuff, Portable automatic cuff pressure controller REF: 951001
View official recall notice →