FDAClass IFebruary 1, 2023

Getinge Flow-c Anesthesia System recall: Software Issue

Getinge Flow-c Anesthesia System, Part No. 6887700

Why was Getinge Flow-c Anesthesia System recalled?

Due to a software bug, under certain conditions, pressure cannot be built up resulting in no ventilation. If gas delivery is stopped, a sustained decrease in delivered O2 concentration may lead to hypoventilation and hypoxia.

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?

Part # UDI 6887700 07325710009765 Serial Numbers 4003-5078 Software versions 4.8.0, 4.8.1, 4.8.2, and 4.8.3.

Product
Getinge Flow-c Anesthesia System, Part No. 6887700
Recalling firm
Getinge Usa Sales Inc
Quantity
8.016 Total (7.766 OUS; 250 US)
Distribution
US nationwide and Worldwide Distribution: Domestic distribution to AL, AR, AZ, CA, CO, DC, FL, GA, IN, MA, MI, MO, NY, OH, OR, PA, TX, VA, WA, WV. Foreign distribution worldwide.
Recall date
February 1, 2023
Classification
Class I
Status
Ongoing
Agency
FDA (device)
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