Class II — Potential Health Hazard

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

MR Patient Care Portal 5000 (Desktop Unit) Recalled by Philips North America Llc Due to Device may intermittently fail to produce audio. Turning...

Date: September 6, 2022
Company: Philips North America Llc
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 Philips North America Llc directly.

Affected Products

MR Patient Care Portal 5000 (Desktop Unit), Model Number 453564792561 This is a component of product number 866162.

Quantity: 115 US; 193 ROW

Why Was This Recalled?

Device may intermittently fail to produce audio. Turning the unit off and on does not resolve the issue; disconnecting and reconnecting to AC power does not reliably resolve the issue.

Where Was This Sold?

This product was distributed to 25 states: AL, AZ, CA, CO, FL, GA, ID, IL, IN, LA, MA, MI, MN, NE, NJ, NC, OH, PA, SC, TN, TX, UT, VT, WA, WY

Affected (25 states)Not affected

About Philips North America Llc

Philips North America Llc has 301 total recalls tracked by RecallDetector.

Related Recalls

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