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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 10 of 25 Results
510(K) Number: K022074
 
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Product Description
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FDA Recall
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BAG 9732315 MOUSE STERILE 15 PK 2 05/09/2014 Medtronic Navigation, Inc.
UPGRD PRGM 9734638 ADD AxiEM NAVIGATION 2 05/09/2014 Medtronic Navigation, Inc.
BIT 9733516 2.9mm DRILL STERILE 2 05/09/2014 Medtronic Navigation, Inc.
DISP 9730950 STRL SPHERE, 1 PK INSERT 2 05/09/2014 Medtronic Navigation, Inc.
DISP 9730951 STRL SPHERE, 5PK INSERT 2 05/09/2014 Medtronic Navigation, Inc.
DRAPE 9732722 TUBE STERILE O-ARM 20PK 2 05/09/2014 Medtronic Navigation, Inc.
ENT PRGM 9734636 ADD FUSION NAV AxiEM 2 05/09/2014 Medtronic Navigation, Inc.
INST 9731132 KIT CR REF FRAME DRIVER 5PK 2 05/09/2014 Medtronic Navigation, Inc.
INSTRUMENT TRACKER 9733533XOM ENT 1PK 2 05/09/2014 Medtronic Navigation, Inc.
KIT, 9731427, THORACIC TACTILE PROBES 2 05/09/2014 Medtronic Navigation, Inc.
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