Smith & Nephew, Inc. Endoscopy Division recalls
Smith & Nephew, Inc. Endoscopy Division has 37 recalls on record with the FDA and USDA, the earliest in 2012 and the latest reported on 23 Jul 2014. The most frequent reason is sterility.
Total recalls 37 since 2012
Last 12 months 0 reported
Class I 0 0% of total
Ongoing 0 latest 23 Jul 2014
Recalls per month, last 24 months click a bar for that month Severity split
0 0%37 100%0 0%
Why smith & nephew, inc. endoscopy division is recalled
All smith & nephew, inc. endoscopy division recalls, newest first 37 total Reported Class Recall Company Reason Where 23 Jul 2014 Device CLASS II Suturefix Ultra Anchor XL recalled by Smith & Nephew, Inc. Smith & Nephew, Inc. Endoscopy Division Sterility Nationwide 23 Jul 2014 Device CLASS II Suturefix Ultra Anchor XL with one (#2) Ultrabraid Blue Product recalled Smith & Nephew, Inc. Endoscopy Division Sterility Nationwide 23 Jul 2014 Device CLASS II Suturefix Ultra S Double Loaded Suture Product recalled Smith & Nephew, Inc. Endoscopy Division Sterility Nationwide 23 Jul 2014 Device CLASS II Suturefix Ultra S with 1 #2 Ultrabraid Suture (blue/white) Product recalled Smith & Nephew, Inc. Endoscopy Division Sterility Nationwide 23 Jul 2014 Device CLASS II Suturefix Ultra S with 1 #2 Ultrabraid (blue) Product recalled Smith & Nephew, Inc. Endoscopy Division Sterility Nationwide 25 Sep 2013 Device CLASS II Twinfix Ultra HA Suture Anchor with 2 Ultrabraid Suture recalled Smith & Nephew, Inc. Endoscopy Division Sterility Nationwide 25 Sep 2013 Device CLASS II Osteoraptor Suture Anchor with Ultrabraid Cobraid Suture, Blue recalled Smith & Nephew, Inc. Endoscopy Division Sterility Nationwide 25 Sep 2013 Device CLASS II Twinfix" Ultra Plla-ha Suture Anchor recalled by Smith & Nephew, Inc. Smith & Nephew, Inc. Endoscopy Division Sterility Nationwide 25 Sep 2013 Device CLASS II Twinfix Ultra Plla-ha Suture Anchor recalled by Smith & Nephew, Inc. Smith & Nephew, Inc. Endoscopy Division Sterility Nationwide 25 Sep 2013 Device CLASS II Osteoraptor Curved Suture Anchor Ultrabraid Cobraid Suture, Black recalled Smith & Nephew, Inc. Endoscopy Division 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.