Total recalls 52 since 2012
Last 12 months 0 reported
Class I 0 0% of total
Ongoing 0 latest 15 Nov 2017
Recalls per month, last 24 months click a bar for that month Severity split
0 0%51 98%1 2%
Why sorin group usa is recalled
All sorin group usa recalls, newest first 52 total Reported Class Recall Company Reason Where 15 Nov 2017 Device CLASS II FlexFlow Venous Cannula recalled by Sorin Group USA Sorin Group USA Sterility Nationwide 16 Aug 2017 Device CLASS II Sorin Group Aortic Arch Cannula x recalled Sorin Group USA Foreign Material Nationwide 9 Aug 2017 Device CLASS II Sorin Group, Smart Perfusion Pack, Smart Venous Vacuum recalled Sorin Group USA Sterility Nationwide 9 Aug 2017 Device CLASS II Sorin Group, Smart Perfusion Pack, Neonate/pediatric Pack recalled Sorin Group USA Sterility Nationwide 9 Aug 2017 Device CLASS II Sterile Sample Sorin Group, Smart Perfusion Pack recalled Sorin Group USA Sterility Nationwide 9 Aug 2017 Device CLASS II Sorin Group, Smart Perfusion Pack, Smart 3/16" Peds Pack recalled Sorin Group USA Sterility Nationwide 9 Aug 2017 Device CLASS II Sorin Group, Smart Perfusion Pack, Long Pack recalled Sorin Group USA Sterility Nationwide 9 Aug 2017 Device CLASS II Non-sterile Sample, Sorin Group, Smart Cardioplegia recalled Sorin Group USA Sterility Nationwide 9 Aug 2017 Device CLASS II Non-sterile Sample, Sorin Group, Smart Perfusion Pack, Inspire 8fs recalled Sorin Group USA Sterility Nationwide 9 Aug 2017 Device CLASS II Sorin Group, Smart Perfusion Pack, Pump And Table Pack recalled Sorin Group USA 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.