🔍 RecallPedia

IntelliVue MX700 patient monitor, model no. 865241

Class I - Dangerous
🏥 Medical Devices Recalled: June 30, 2020 Philips North America Diagnostic Equipment

What Should You Do?

  1. Check if you have this product:
    Serial numbers DE58562415 DE58562344 DE58562353
  2. Do not eat it: Even if it looks and smells fine, do not consume this product.
  3. Throw it away or return it: You can return the product to the store for a full refund.
  4. Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
  5. Report problems: Report any issues to the FDA's Safety Reporting Portal.

⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.

Recall Details

Company:
Philips North America, LLC
Reason for Recall:
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.
Classification:
Class I - Dangerous

Dangerous or defective products that predictably could cause serious health problems or death.

Status:
terminated

Product Information

Full Description:

IntelliVue MX700 patient monitor, model no. 865241

Product Codes/Lot Numbers:

Serial numbers DE58562415 DE58562344 DE58562353

Distribution:

Distributed in: CA, HI, MA, NY, UT

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-2697-2020

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