System, Balloon, Intra-aortic And Control
Arrow International, Llc (subsidiary Of Teleflex, Incorporated)'s record for this product code
MDR events86All time
Recalls0All time
510(k) clearances0All time
Recent MDR events
86 adverse event reports on file
- ARROW IABPJun 17, 2026MalfunctionMW5189541
- TERAFLEX IABPJun 9, 2026OtherMW5189051
- TERAFLEX IABPJun 9, 2026OtherMW5189052
- ARROW TELEFLEXJun 1, 2026MalfunctionMW5188768
- FIBEROPTIX IAB CATHETERMay 7, 2026MalfunctionMW5187863
- INTRA-AORTIC BALLOONMay 7, 2026InjuryMW5187874
- TELEFLEX FIBEROPTIX IABApr 29, 2026InjuryMW5187435
- CIRCULATORY ASSIST UNITApr 28, 2026MalfunctionMW5187397
- INTRA-AORTIC BALLOON PUMPApr 27, 2026MalfunctionMW5187268
- TELEFLEX FIBEROPTIX IAB CATHETERApr 1, 2026MalfunctionMW5186244
Recalls
0 recall events for this product code
No recalls on file for Arrow International, Llc (subsidiary Of Teleflex, Incorporated) under this product code.
510(k) clearances
0 clearances for this product code
No 510(k) clearances on file for Arrow International, Llc (subsidiary Of Teleflex, Incorporated) under this product code.