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U.S. Department of Health and Human Services

Medical Device Recalls
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510(K) Number: K903205
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FDA Recall
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Covidien Endo Clinch II Auto Suture Grasper, 5mm REF: 174317 The Covidien Endo Clinch" II Auto... 2 04/23/2019 COVIDIEN LLC
Procedure kits include devices from the affected lots distributed OUS only: (1)BOX KIT00529H KIT CO... 2 04/23/2019 COVIDIEN LLC
Covidien Endo Grasp Auto Suture Grasper 5mm REF: 173030 The Covidien Endo Grasp" Auto Suture" gr... 2 04/23/2019 COVIDIEN LLC
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