Class I Recall: Arrow International Intra-Aortic Balloon Catheter Kits and Percutaneous Insertion Kits by Teleflex - Sheath Body may become Separated from Sheath Hub

Class I Recall: Arrow International Intra-Aortic Balloon Catheter Kits and Percutaneous Insertion Kits by Teleflex - Sheath Body may become Separated from Sheath Hub

Teleflex Incorporated announces worldwide recall of Arrow International Intra-Aortic Balloon Catheter Kits and Percutaneous Insertion Kits. More information

Helene Clayton-Jeter, O.D.
Office of Health and Constituent Affairs
Food and Drug Administration

For more information about the Cardiovascular & Endocrine Liaison Program visit the FDA Patient Network