🔍 RecallPedia

IntelliVue G7m Anesthesia Gas Module, Product Number 866173

Class I - Dangerous
🏥 Medical Devices Recalled: January 18, 2023 Philips North America Infusion Pumps Nationwide

What Should You Do?

  1. Check if you have this product:
    UDI-DI: 00884838051492; Serial Numbers: DE43800129 through DE43812627
  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
Reason for Recall:
The 866173 lntelliVue G7m Anesthesia Gas Modules could have a component issue that may trigger an interruption of the gas measurement. This issue concerns the G7m's sample gas pump which could stop working, producing a technical, INOP (inoperable) alarm. The pump may fail prematurely when there is friction caused by an abrasion. This recall is for an IMPORTANT PRODUCT NOTICE dated 1/18/23.
Classification:
Class I - Dangerous

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

Status:
ongoing

Product Information

Full Description:

IntelliVue G7m Anesthesia Gas Module, Product Number 866173

Product Codes/Lot Numbers:

UDI-DI: 00884838051492; Serial Numbers: DE43800129 through DE43812627

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-0007-2025

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