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U.S. Department of Health and Human Services

Medical Device Recalls
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101 to 110 of 500 Results *
Recall Date from: 01/01/2016 Recall Date to: 06/13/2016
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Product Description
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Recall
Class
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FDA Recall
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American Surgical Ultracot 6 mm x 50 mm Ref Number: 23-06 Product Usage: Neurosurgical and Nonne... 2 05/26/2016 American Surgical Company
American Surgical Ultracot 9 mm x 50 mm (Glassine) Ref Number: 23-07G Product Usage: Neurosurgic... 2 05/26/2016 American Surgical Company
American Surgical Ultracot 13 mm x 60 mm Ref Number: 23-08 Product Usage: Neurosurgical and Nonn... 2 05/26/2016 American Surgical Company
American Surgical Ultracot 13 mm x 60 mm (Glassine) Ref Number: 23-08G Product Usage: Neurosurgic... 2 05/26/2016 American Surgical Company
American Surgical Ultracot 20 mm x 60 mm Ref Number: 23-09 Product Usage: Neurosurgical and Nonn... 2 05/26/2016 American Surgical Company
American Surgical Ultracot 20 mm x 60 mm (Glassine) Ref Number: 23-09G Product Usage: Neurosurgic... 2 05/26/2016 American Surgical Company
American Surgical Ultracot 30 mm x 70 mm Ref Number: 23-10 Product Usage: Neurosurgical and No... 2 05/26/2016 American Surgical Company
American Surgical Ultracot 30 mm x 70 mm (Glassine) Ref Number: 23-10G Product Usage: Neurosurgic... 2 05/26/2016 American Surgical Company
American Surgical Ultracot 15 mm x 15 mm (Glassine) Ref Number: 23-12G Product Usage: Neurosurgic... 2 05/26/2016 American Surgical Company
American Surgical Ultracot 30 mm x 90 mm (Glassine) Ref Number: 23-15G Product Usage: Neurosurgic... 2 05/26/2016 American Surgical Company

*   The maximium 500 devices meeting your search criteria returned. Please narrow your search.
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