Total recalls 17 since 2013
Last 12 months 0 reported
Class I 0 0% of total
Ongoing 0 latest 25 Dec 2013
Recalls per month, last 24 months click a bar for that month Severity split
0 0%17 100%0 0%
Why karl storz endoscopy america is recalled
All karl storz endoscopy america recalls, newest first 17 total Reported Class Recall Company Reason Where 25 Dec 2013 Device CLASS II Intubation Flexible Fiberscope recalled by Karl Storz Endoscopy America Karl Storz Endoscopy America Foreign Material Nationwide 25 Dec 2013 Device CLASS II Broncho Flexible Fiberscope recalled by Karl Storz Endoscopy America Karl Storz Endoscopy America Foreign Material Nationwide 18 Dec 2013 Device CLASS II Axillent Debakey Grasping Forceps recalled Karl Storz Endoscopy America Labeling Errors Nationwide 24 Jul 2013 Device CLASS II 27023WU Balloon Catheter., 2/pkg, sterile, contains latex recalled Karl Storz Endoscopy America Sterility 5 states 22 May 2013 Device CLASS II Electrode, Barrel Bar (27050NX/6) recalled Karl Storz Endoscopy America Sterility Nationwide 22 May 2013 Device CLASS II Loop, Cutting/6) recalled by Karl Storz Endoscopy America Karl Storz Endoscopy America Sterility Nationwide 22 May 2013 Device CLASS II Electrode, Coag, Ball End (27050N/6) recalled Karl Storz Endoscopy America Sterility Nationwide 22 May 2013 Device CLASS II Electrode, cutting-.30/6) recalled by Karl Storz Endoscopy America Karl Storz Endoscopy America Sterility Nationwide 22 May 2013 Device CLASS II Knife, Cold, Straight (27068K/6) recalled Karl Storz Endoscopy America Sterility Nationwide 22 May 2013 Device CLASS II Loop, Cutting, Angled/6) recalled by Karl Storz Endoscopy America Karl Storz Endoscopy America Sterility Nationwide
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About this list
Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.