Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K101778 |
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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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Giraffe Incubator with installed Servo Oxygen module. Infant incubator. | 2 | 06/15/2020 | GE Healthcare, LLC |
Giraffe OmniBed® and Giraffe Incubator p/n 6600-0723-700 (rev A and B) labeled in part: ***GE Healt... | 1 | 04/05/2013 | GE Healthcare, LLC |
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