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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 6 of 6 Results
510(K) Number: K122059
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Product Description
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FDA Recall
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SUTUREFIX ULTRA Suture, Product number 72203855 2 07/31/2020 Smith & Nephew, Inc.
SUTUREFIX Ultra Anchor XL with one (#2) Ultrabraid Cobraid Suture Product Code: 72203842 Fastene... 2 07/14/2014 Smith & Nephew, Inc. Endoscopy Division
SUTUREFIX Ultra S with 1 #2 Ultrabraid Suture (blue/white) Product Code: 72203853 Fastener, fixa... 2 07/14/2014 Smith & Nephew, Inc. Endoscopy Division
SUTUREFIX Ultra S Double Loaded Suture Product Code: 72203854 Fastener, fixation, nondegradable,... 2 07/14/2014 Smith & Nephew, Inc. Endoscopy Division
SUTUREFIX Ultra Anchor XL with one (#2) Ultrabraid Blue Product Code: 72203841 Fastener, fixat... 2 07/14/2014 Smith & Nephew, Inc. Endoscopy Division
SUTUREFIX Ultra S with 1 #2 Ultrabraid (blue) Product Code: 72203852 Fastener, fixation, nondegr... 2 07/14/2014 Smith & Nephew, Inc. Endoscopy Division
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