Brand

Arrow International, Inc., Division Of Teleflex Medical Inc. Recalls

6 recalls on record. Search official CPSC, FDA, and USDA datasets for every recall issued for Arrow International, Inc., Division Of Teleflex Medical Inc..

6Total Recalls
6Critical
80,430Units Affected
Feb 10, 2016Most Recent
All Recalls

Every Arrow International, Inc., Division Of Teleflex Medical Inc. Recall

Sorted by most recent. Click any recall for full details.

6 recalls
CriticalFDA
Arrow International, Inc., Division Of Teleflex Medical Inc.
Percutaneous Insertion Tray; Product Code: IAK-06845 The Arrow¿ IAB is utilized for intra aortic balloon counterpulsation therapy in t...
Cardiac Devices·13,405 affected·Feb 10, 2016
CriticalFDA
Arrow International, Inc., Division Of Teleflex Medical Inc.
Ultra 8 IAB: 8Fr 40cc; Product Code: IAB-05840-U The Arrow¿ IAB is utilized for intra aortic balloon counterpulsation therapy in the a...
Cardiac Devices·13,405 affected·Feb 10, 2016
CriticalFDA
Arrow International, Inc., Division Of Teleflex Medical Inc.
Ultra 8 IAB: 8Fr 30cc; Product Code: IAB-05830-U The Arrow¿ IAB is utilized for intra aortic balloon counterpulsation therapy in the a...
Cardiac Devices·13,405 affected·Feb 10, 2016
CriticalFDA
Arrow International, Inc., Division Of Teleflex Medical Inc.
RediGuard IAB: 7Fr 30cc; Product Code: IAB-S730C The Arrow¿ IAB is utilized for intra aortic balloon counterpulsation therapy in the a...
Cardiac Devices·13,405 affected·Feb 10, 2016
CriticalFDA
Arrow International, Inc., Division Of Teleflex Medical Inc.
UltraFlex IAB: 7.5Fr 30cc; Product Code: IAB-06830-U The Arrow¿ IAB is utilized for intra aortic balloon counterpulsation therapy in t...
Cardiac Devices·13,405 affected·Feb 10, 2016
CriticalFDA
Arrow International, Inc., Division Of Teleflex Medical Inc.
FiberOptix Ultra 8 IAB: 8Fr 30cc The Arrow¿ IAB is utilized for intra aortic balloon counterpulsation therapy in the aorta, whereby ba...
Cardiac Devices·13,405 affected·Feb 10, 2016