Class II — Potential Health Hazard

Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.

Intellicuff Standalone (PN 951001) Used to continuously measure and automatically Recalled by Hamilton Medical, Inc. Due to Issue related to the performance of the motor...

Date: June 20, 2017
Company: Hamilton Medical, Inc.
Status: Ongoing
Source: FDA (Device)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact Hamilton Medical, Inc. directly.

Affected Products

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.

Quantity: 176 units

Why Was This Recalled?

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

Where Was This Sold?

This product was distributed to 2 states: IL, TX

Affected (2 states)Not affected

About Hamilton Medical, Inc.

Hamilton Medical, Inc. has 19 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Device). Last updated March 26, 2026. View original report