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U.S. Department of Health and Human Services

Medical Device Recalls
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510(K) Number: K981329
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Recall
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NEO-KATH(TM) Caudal Set, REF 201-2430, Sterile 2 08/18/2021 Epimed International
NEO-KATH Epidural Catheter Set, REF 200-2430, Sterile 2 08/18/2021 Epimed International
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