ARROWRecalls & reported problems across all models
Teleflex Incorporated · 1,494 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
ARROW models — page 2
1,494 models, 100 per page, most reported first. Each model has its own page with its reports, recalls and device details.
- ARROW IPN922908Catheter, intravascular, therapeutic, short-term less than 30 days2 recalls0 reports
- ARROW IPN922906INSTRUMENT, BIOPSY2 recalls0 reports
- ARROW IPN923103Catheter, intravascular, therapeutic, short-term less than 30 days2 recalls0 reports
- ARROW IPN923182Catheter, percutaneous2 recalls0 reports
- ARROW IPN924180Catheter, intravascular, therapeutic, long-term greater than 30 days2 recalls0 reports
- ARROW IPN924181Catheter, intravascular, therapeutic, long-term greater than 30 days2 recalls0 reports
- ARROW IPN924975CATHETER, CONDUCTION, ANESTHETIC2 recalls0 reports
- ARROW IPN925020CATHETER, CONDUCTION, ANESTHETIC2 recalls0 reports
- ARROW IPN925052CATHETER, CONDUCTION, ANESTHETIC2 recalls0 reports
- ARROW IPN925200Wire, guide, catheter2 recalls0 reports
- ARROW IPN926611Introducer, catheter2 recalls0 reports
- ARROW IPN927215Wire, guide, catheter2 recalls0 reports
- ARROW IPN927343Catheter, hemodialysis, non-implanted2 recalls0 reports
- ARROW IPN927550Catheter, intravascular, therapeutic, short-term less than 30 days2 recalls0 reports
- ARROW IPN927743CATHETER, CONDUCTION, ANESTHETIC2 recalls0 reports
- ARROW IPN927740Catheter, intravascular, therapeutic, short-term less than 30 days2 recalls0 reports
- ARROW IPN928638Catheter, intravascular, therapeutic, long-term greater than 30 days2 recalls0 reports
- ARROW IPN929229Introducer, catheter2 recalls0 reports
- ARROW IPNB00178Catheter, intravascular, therapeutic, short-term less than 30 days2 recalls0 reports
- ARROW IPNB00181Catheter, intravascular, therapeutic, short-term less than 30 days2 recalls0 reports
- ARROW IPNB00182Catheter, intravascular, therapeutic, short-term less than 30 days2 recalls0 reports
- ARROW IPNB00180Catheter, intravascular, therapeutic, short-term less than 30 days2 recalls0 reports
- ARROW IPN036604Catheter, percutaneous2 recalls0 reports
- ARROW IPN036856Syringe, piston2 recalls0 reports
- ARROW IPN036419CATHETER, HEMODIALYSIS, NON-IMPLANTED2 recalls0 reports
- ARROW IPN036986CATHETER, PERITONEAL2 recalls0 reports
- ARROW IPN029798Wire, guide, catheter2 recalls0 reports
- ARROW IPN055749Wire, guide, catheter2 recalls0 reports
- ARROW IPN922619CATHETER, CONDUCTION, ANESTHETIC2 recalls0 reports
- ARROW IPN036186CATHETER, HEMODIALYSIS, TRIPLE LUMEN, NON-IMPLANTED2 recalls0 reports
- ARROW IPN036456Catheter, intravascular, therapeutic, short-term less than 30 days2 recalls0 reports
- ARROW IPN036428CATHETER, HEMODIALYSIS, NON-IMPLANTED2 recalls0 reports
- ARROW IPN915614Catheter, intravascular, therapeutic, short-term less than 30 days1 recall48 reports
- ARROW IPN035912WIRE, GUIDE, CATHETER92 reports
- ARROW IPN036043CATHETER, PERCUTANEOUS88 reports
- ARROW IPN036437Catheter,intravascular,therapeutic,short-term less than 30 days1 recall33 reports
- ARROW IPN915667Needle, hypodermic, single lumen1 death80 reports
- ARROW IPN915322System, balloon, intra-aortic and control1 recall29 reports
- ARROW IPN923013Catheter, intravascular, therapeutic, long-term greater than 30 days1 recall25 reports
- ARROW IPN037306Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall25 reports
- ARROW IPN035916WIRE, GUIDE, CATHETER73 reports
- ARROW IPN036984Wire, guide, catheter1 recall23 reports
- ARROW IPN030129Catheter,intravascular,therapeutic,short-term less than 30 days71 reports
- ARROW IPN033036Catheter, hemodialysis, implanted1 death70 reports
- ARROW IPN033424Catheter,intravascular,therapeutic,long-term greater than 30 days70 reports
- ARROW IPN917235CATHETER, FLOW DIRECTED69 reports
- ARROW IPN924166Catheter, intravascular, therapeutic, long-term greater than 30 days1 recall18 reports
- ARROW IPN915319System, balloon, intra-aortic and control1 recall17 reports
- ARROW IPN924172Catheter, intravascular, therapeutic, long-term greater than 30 days1 recall13 reports
- ARROW IPN037072Catheter,intravascular,therapeutic,short-term less than 30 days1 recall13 reports
- ARROW IPN035902CATHETER, EMBOLECTOMY1 recall12 reports
- ARROW IPN030147CATHETER, HEMODIALYSIS, NON-IMPLANTED62 reports
- ARROW IPN039793System, balloon, intra-aortic and control62 reports
- 1 recall12 reports
- ARROW IPN000252System, balloon, intra-aortic and control61 reports
- ARROW IPN924169Catheter, intravascular, therapeutic, long-term greater than 30 days1 recall11 reports
- ARROW IPN030090Catheter, hemodialysis, triple lumen, non-implanted60 reports
- ARROW IPN927347Catheter, hemodialysis, non-implanted1 recall10 reports
- ARROW IPN915619Catheter, intravascular, therapeutic, short-term less than 30 days1 recall1 death9 reports
- 1 recall9 reports
- ARROW IPN924171Catheter, intravascular, therapeutic, long-term greater than 30 days1 recall9 reports
- ARROW IPN037698Midline catheter1 recall9 reports
- ARROW IPN915623Catheter, intravascular, therapeutic, short-term less than 30 days1 recall8 reports
- ARROW IPN916138System, balloon, intra-aortic and control1 recall8 reports
- ARROW IPN924163Catheter, intravascular, therapeutic, long-term greater than 30 days1 recall8 reports
- ARROW IPN915321System, balloon, intra-aortic and control1 recall7 reports
- 57 reports
- ARROW IPN929210System, balloon, intra-aortic and control57 reports
- ARROW IPN033108Catheter, hemodialysis, implanted1 recall7 reports
- ARROW IPN037160Wire, guide, catheter1 recall7 reports
- ARROW IPN036455Catheter, intravascular, therapeutic, short-term less than 30 days1 recall7 reports
- ARROW IPN036826INTRODUCER, CATHETER1 recall6 reports
- ARROW IPN915621Catheter, intravascular, therapeutic, short-term less than 30 days1 recall6 reports
- ARROW IPN920475Catheter, hemodialysis, implanted1 recall6 reports
- ARROW IPN921746Wire, guide, catheter1 recall6 reports
- ARROW IPN924156Catheter, intravascular, therapeutic, long-term greater than 30 days1 recall6 reports
- ARROW IPN924170Catheter, intravascular, therapeutic, long-term greater than 30 days1 recall6 reports
- ARROW IPN036440Catheter,intravascular,therapeutic,short-term less than 30 days1 recall6 reports
- ARROW IPN920509Catheter, hemodialysis, implanted1 recall5 reports
- ARROW IPN923012Catheter, intravascular, therapeutic, long-term greater than 30 days1 recall5 reports
- ARROW IPN924157Catheter, intravascular, therapeutic, long-term greater than 30 days1 recall5 reports
- ARROW IPN925080Wire, guide, catheter1 recall5 reports
- ARROW IPN036444INTRODUCER, CATHETER1 recall5 reports
- ARROW IPN036514Wire, guide, catheter1 recall5 reports
- ARROW IPN920517Catheter, hemodialysis, implanted1 recall1 death5 reports
- ARROW IPN036421Catheter, intravascular, therapeutic, long-term greater than 30 days1 recall5 reports
- ARROW IPN036979INTRODUCER, CATHETER1 recall4 reports
- ARROW IPN036982WIRE, GUIDE, CATHETER1 recall4 reports
- ARROW IPN037859Catheter,intravascular,therapeutic,short-term less than 30 days1 recall4 reports
- ARROW IPN038527Catheter, intravascular, therapeutic, short-term less than 30 days1 recall4 reports
- ARROW IPN029789Catheter, intravascular, therapeutic, short-term less than 30 days1 recall4 reports
- ARROW IPN915317System, balloon, intra-aortic and control1 recall4 reports
- ARROW IPN921747Wire, guide, catheter1 recall4 reports
- ARROW IPN924159Catheter, intravascular, therapeutic, long-term greater than 30 days1 recall4 reports
- ARROW IPN924966CATHETER, CONDUCTION, ANESTHETIC1 recall4 reports
- ARROW IPN927748Saline, vascular access flush1 recall4 reports
- ARROW IPN000302System, balloon, intra-aortic and control54 reports
- ARROW IPN037302Catheter, intravascular, therapeutic, long-term greater than 30 days1 recall4 reports
- ARROW IPN035619Catheter,intravascular,therapeutic,short-term less than 30 days1 recall3 reports
- ARROW IPN036335INTRODUCER, CATHETER1 recall3 reports
Sources and updates
- Models: FDA GUDID, file dated Oct 13, 2026. Models are grouped by the brand name the manufacturer registered.
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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