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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 3 of 3 Results
510(K) Number: K032701
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Product Description
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Recall
Class
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FDA Recall
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Recalling Firm
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Circular Stapler 21 mm Digital Loading Unit, product code CS21; Circular Stapler 25 mm Digital Loadi... 2 11/23/2009 Surgical Devices/Covidien
SurgAssist System Circular Stapler DLU 29mm 2 12/19/2003 Power Medical Interventions
SurgAssist System Circular Stapler DLU 33mm 2 12/19/2003 Power Medical Interventions
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