Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K030691 |
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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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Philips Fetal Spiral Electrode-intended for patients requiring fetal heart rate monitoring during la... | 2 | 01/06/2023 | Philips North America Llc |
Fetal Spiral Electrode, Model No. 9898 031 37631 | 2 | 05/02/2019 | Philips North America, LLC |
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