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www.fdanews.com/articles/186766-dr%C3%A4ger-medical-recalls-fabius-anesthesia-machines
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Dräger Medical Recalls Fabius Anesthesia Machines

May 11, 2018

Dräger recalled its Fabius anesthesia machine products, including its GS Premium, Tiro, Tiro M and MRI anesthesia machines.

The FDA classified the recall as Class I and warned that use of the machines could cause serious injury or death.

The Fabius products are inhalation anesthesia machines used in operating, induction and recovery rooms in hospitals and MRI settings for patients of all ages.

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