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Hamilton Medical, Inc. recalls Intellicuff Standalone (PN 951001) Used to continuously measure and automatically maintain the user-set cuff pressure
Recalled January 24, 2018 · FDA recall Z-0335-2018 · Hamilton Medical
Hazard
Issue related to the performance of the motor in recalled product. During use, motor may cease to function. · FDA Class II
Units
176 units
Sold at
US Distribution to IL and TX.
Description
Issue related to the performance of the motor in recalled product. During use, motor may cease to function.
Product
Intellicuff Standalone (PN 951001) Used to continuously measure and automatically maintain the user-set cuff pressure of an endotracheal tube or tracheostomy tube during mechanical ventilation. Used in the ventilation of adults, pediatrics, and neonates.
Manufacturer(s)
Hamilton Medical, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →