FDAJune 20, 2017device

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.

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Issue related to the performance of the motor in recalled product. During use, motor may cease to function.

What to do

FDA enforcement status: Ongoing

Brands named

hamilton medicalhamilton

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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