Philips North America: Medical Device Recall in 2024 - (Recall #: Z-0007-2025)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2024.

Data Source: FDA.

Product Description:

IntelliVue G7m Anesthesia Gas Module, Product Number 866173

Product Classification:

Class II

Date Initiated: January 18, 2023

Date Posted: October 9, 2024

Recall Number: Z-0007-2025

Event ID: 95301

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.

Status: Ongoing

Product Quantity: 8,449 devices

Code Information:

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

Distribution Pattern:

US Nationwide. Global Distribution.

Voluntary or Mandated:

Voluntary: Firm initiated