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U.S. Department of Health and Human Services

Medical Device Recalls

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1 result found
510(K) Number: K181134
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Product Description
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Recall
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FDA Recall
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Recalling Firm
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SUNSTAR G.U.M. HYDRAL DRY MOUTH RELIEF On-the-go Oral Spray, 2 FL.OZ. UPC0 70942 30713 0 - Product U... 2 03/05/2021 Sunstar Americas, Inc.
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