Arrow International, Inc., Division of Teleflex Medical recalls
Arrow International, Inc., Division of Teleflex Medical has 9 recalls on record with the FDA and USDA, the earliest in 2016 and the latest reported on 16 Mar 2016.
Total recalls 9 since 2016
Last 12 months 0 reported
Class I 9 100% of total
Ongoing 0 latest 16 Mar 2016
Recalls per month, last 24 months click a bar for that month Severity split
9 100%0 0%0 0%
Why arrow international, inc., division of teleflex medical is recalled
All arrow international, inc., division of teleflex medical recalls, newest first 9 total Reported Class Recall Company Reason Where 16 Mar 2016 Device CLASS I FiberOptix Ultra 8 IAB: 40cc recalled by Arrow International, Inc. Arrow International, Inc., Division of Teleflex Medical Other Nationwide 16 Mar 2016 Device CLASS I Percutaneous Insertion Tray recalled by Arrow International, Inc. Arrow International, Inc., Division of Teleflex Medical Other Nationwide 16 Mar 2016 Device CLASS I UltraFlex IAB recalled by Arrow International, Inc. Arrow International, Inc., Division of Teleflex Medical Other Nationwide 16 Mar 2016 Device CLASS I FiberOptix Ultra 8 IAB: 30cc The Arrow¿ IAB is utilized recalled Arrow International, Inc., Division of Teleflex Medical Other Nationwide 16 Mar 2016 Device CLASS I UltraFlex IAB recalled by Arrow International, Inc. Arrow International, Inc., Division of Teleflex Medical Other Nationwide 16 Mar 2016 Device CLASS I RediGuard IAB: 30cc recalled by Arrow International, Inc. Arrow International, Inc., Division of Teleflex Medical Other Nationwide 16 Mar 2016 Device CLASS I Ultra 8 IAB: 30cc recalled by Arrow International, Inc. Arrow International, Inc., Division of Teleflex Medical Other Nationwide 16 Mar 2016 Device CLASS I Ultra 8 IAB: 40cc recalled by Arrow International, Inc. Arrow International, Inc., Division of Teleflex Medical Other Nationwide 16 Mar 2016 Device CLASS I Percutaneous Insertion Tray recalled by Arrow International, Inc. Arrow International, Inc., Division of Teleflex Medical Other Nationwide
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.