IntelliVue G7m Anesthesia Gas Module recall
IntelliVue G7m Anesthesia Gas Module, Product Number 866173
Why was IntelliVue G7m Anesthesia Gas Module recalled?
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.
What should I do if I have this product?
The recall is ongoing. Follow the firm and FDA instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
UDI-DI: 00884838051492; Serial Numbers: DE43800129 through DE43812627
- Product
- IntelliVue G7m Anesthesia Gas Module, Product Number 866173
- Recalling firm
- Philips North America
- Quantity
- 8,449 devices
- Distribution
- US Nationwide. Global Distribution.
- Recall date
- October 9, 2024
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)