FDAJuly 12, 2024device

Aespire 7100, 7100 (Variant), and Aespire 7100 S/5 Protiva configurations. These anesthesia gas machines are intended to provide general inhalation anesthesia and ventilatory support to patients and are to be used only by medical professionals trained and qualified in the administration of genera...

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Potential issue that may arise if the limb of a patient breathing circuit is mistakenly connected to the Auxiliary Common Gas Outlet (ACGO) port.

What to do

FDA enforcement status: Ongoing

Brands named

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UPCs

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Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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