Medical Device Recalls
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1 result found
510(K) Number: K040044 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Heel Snuggler, Reference # 989805603411 99047 | 2 | 01/19/2022 |
FEI # 3016618143 Philips North America Llc |
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