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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 6 of 6 Results
510(K) Number: K926477
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Product Description
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FDA Recall
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CORE® Suction Irrigation Handpiece with 5mm x 32cm Length Probe for Single Solution or Dual Bags, C... 2 10/18/2016 FEI # 3001451571
ConMed Corporation
CORE® Suction Irrigation Handpiece with 5mm x 32cm Length Probe for Single Solution Bags, Catalog Nu... 2 10/18/2016 FEI # 3001451571
ConMed Corporation
CORE® Suction Irrigation Handpiece without Probe for Single Solution Bags, Catalog Number CD8300 Th... 2 10/18/2016 FEI # 3001451571
ConMed Corporation
CORE® Suction Irrigation Handpiece without Probe for Single Solution or Dual Bags, Catalog Number CD... 2 10/18/2016 FEI # 3001451571
ConMed Corporation
CORE® Trumpet Handpiece only, Catalog Number CD8450 The CORE Trumpet (CD81XX, CD83XX, and CD84XX) h... 2 10/18/2016 FEI # 3001451571
ConMed Corporation
CORE® Trumpet Handpiece with 5mm x 32cm Length Probe , Catalog Number CD8400 The CORE Trumpet (CD81... 2 10/18/2016 FEI # 3001451571
ConMed Corporation
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