Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K123195 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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CARESCAPE Respiratory Module E-sCO | 1 | 01/10/2020 | GE Healthcare, LLC |
CARESCAPE Respiratory Module E-sCAiOV | 1 | 01/10/2020 | GE Healthcare, LLC |
CARESCAPE Respiratory Module E-sCAiO | 1 | 01/10/2020 | GE Healthcare, LLC |
CARESCAPE Respiratory Modules E-sCO, E-sCOV, E-sCAiO, E-sCAiOV, E-sCAiOE, E-sCAiOVE; the Airway Gas ... | 2 | 09/09/2014 | GE Healthcare, LLC |
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