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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K072873
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Product Description
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Recall
Class
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FDA Recall
Posting Date
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Recalling Firm
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dS Breast 16ch 1.5T 2 11/25/2024 Philips North America Llc
Mammotrak Diagnostic Coil 3.0T 2 11/25/2024 Philips North America Llc
Mammotrak Diagnostic Coil 1.5T 2 11/25/2024 Philips North America Llc
dS Breast 16ch 3.0T 2 11/25/2024 Philips North America Llc
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