Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
IntelliVue MX700 patient monitor Recalled by Philips North America, LLC Due to Some Intellivue MX700/MX800 Patient Monitors were delivered with...
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
IntelliVue MX700 patient monitor, model no. 865241
Quantity: 28
Why Was This Recalled?
Some Intellivue MX700/MX800 Patient Monitors were delivered with defective power supplies. The defective power supplies might energize the metal parts of monitor if the grounding instructions were not followed, and may also cause the monitor to stop operating or prevent it from being switched on.
Where Was This Sold?
This product was distributed to 5 states: CA, HI, MA, NY, UT
About Philips North America, LLC
Philips North America, LLC has 88 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report