Arrow International, Inc., Division of Teleflex Medical Inc. recalls

9 recalls on record · latest: February 10, 2016

Official U.S. recall history for Arrow International, Inc., Division of Teleflex Medical Inc., compiled from official government records.

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Arrow International, Inc., Division of Teleflex Medical Inc. recalls Percutaneous Insertion Tray; Product Code: IAK-06845 The Arrow¿ IAB is utilized for intra aortic balloon counterpulsati…

February 10, 2016 · Medical device recalls High risk The sheath body may become separated from the sheath hub. If the separation occ…

Arrow International, Inc., Division of Teleflex Medical Inc. recalls Ultra 8 IAB: 8Fr 40cc; Product Code: IAB-05840-U The Arrow¿ IAB is utilized for intra aortic balloon counterpulsation t…

February 10, 2016 · Medical device recalls High risk The sheath body may become separated from the sheath hub. If the separation occ…

Arrow International, Inc., Division of Teleflex Medical Inc. recalls Ultra 8 IAB: 8Fr 30cc; Product Code: IAB-05830-U The Arrow¿ IAB is utilized for intra aortic balloon counterpulsation t…

February 10, 2016 · Medical device recalls High risk The sheath body may become separated from the sheath hub. If the separation occ…

Arrow International, Inc., Division of Teleflex Medical Inc. recalls RediGuard IAB: 7Fr 30cc; Product Code: IAB-S730C The Arrow¿ IAB is utilized for intra aortic balloon counterpulsation t…

February 10, 2016 · Medical device recalls High risk The sheath body may become separated from the sheath hub. If the separation occ…

Arrow International, Inc., Division of Teleflex Medical Inc. recalls UltraFlex IAB: 7.5Fr 30cc; Product Code: IAB-06830-U The Arrow¿ IAB is utilized for intra aortic balloon counterpulsati…

February 10, 2016 · Medical device recalls High risk The sheath body may become separated from the sheath hub. If the separation occ…

Arrow International, Inc., Division of Teleflex Medical Inc. recalls FiberOptix Ultra 8 IAB: 8Fr 30cc The Arrow¿ IAB is utilized for intra aortic balloon counterpulsation therapy in the ao…

February 10, 2016 · Medical device recalls High risk The sheath body may become separated from the sheath hub. If the separation occ…

Arrow International, Inc., Division of Teleflex Medical Inc. recalls UltraFlex IAB: 7.5Fr 40cc; Product Code: IAB-06840-U The Arrow¿ IAB is utilized for intra aortic balloon counterpulsati…

February 10, 2016 · Medical device recalls High risk The sheath body may become separated from the sheath hub. If the separation occ…

Arrow International, Inc., Division of Teleflex Medical Inc. recalls Percutaneous Insertion Tray; Product Code: IAK-S7IT The Arrow¿ IAB is utilized for intra aortic balloon counterpulsatio…

February 10, 2016 · Medical device recalls High risk The sheath body may become separated from the sheath hub. If the separation occ…

Arrow International, Inc., Division of Teleflex Medical Inc. recalls FiberOptix Ultra 8 IAB: 8Fr 40cc; Product Code: IAB-05840-LWS The Arrow¿ IAB is utilized for intra aortic balloon count…

February 10, 2016 · Medical device recalls High risk The sheath body may become separated from the sheath hub. If the separation occ…