FDA MedWatch - Covidien Oridion Labeled Capnostream 20 and Capnostream 20p Patient Monitor Battery Packs by Medtronic: Recall - Risk of Thermal Damage
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Subject
: FDA MedWatch - Covidien Oridion Labeled Capnostream 20 and Capnostream 20p Patient Monitor Battery Packs by Medtronic: Recall - Risk of Thermal Damage
From
: "FDA MedWatch" <fda@xxxxxxxxxxxxxxxxxxxxxxx>
Date
: Wed, 20 Apr 2016 15:44:44 -0500
MedWatch logoMedWatch - The FDA Safety Information and Adverse Event Reporting Program //
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Medtronic Announces Worldwide Voluntary Recall for Battery Pack In Covidien Oridion Labeled Capnostream20 and Capnostream20p Patient Monitors
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