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U.S. Department of Health and Human Services

Medical Device Recalls

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11 to 19 of 19 Results
Class 1 Recall Date from: 01/01/2020 Recall Date to: 02/10/2020
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Product Description
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Recall
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FDA Recall
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Carestation 620/650/650c A1 Product Usage: anesthesia systems are intended to provide general inh... 1 01/23/2020 GE Healthcare, LLC
Carestation 620/650/650c A2 Product Usage: anesthesia systems are intended to provide general inh... 1 01/23/2020 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 Module E-sCOVX 1 01/10/2020 GE Healthcare, LLC
CARESCAPE Respiratory Module E-sCO 1 01/10/2020 GE Healthcare, LLC
Airway Gas Option N-CAiO 1 01/10/2020 GE Healthcare, LLC
CARESCAPE Respiratory Module E-sCAiOVE 1 01/10/2020 GE Healthcare, LLC
CARESCAPE Respiratory Module E-sCAiOE 1 01/10/2020 GE Healthcare, LLC
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