Medical Device Recalls
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1 to 6 of 6 Results
510(K) Number: K122059 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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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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