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Teleflex, and Arrow International, Recall Pressure Injectable Catheter Kits for Mislabeling

Published: November 7, 2023

The FDA has identified this as a Class I recall, the most serious type of recall. Use of these devices may cause serious injuries or death. 

Source: dicardiology.com

Related Topics:

Harrow InternationalCustomer ServiceTeleflex Customer ServiceDrug AdministrationArrow International Pressure Injectable Catheter KitsPressure Injectable Catheter KitsPressure Injectable CatheterPressure Injectable Central Venous CathetersTracker StyletInjectable Catheter KitsUrgent Medical Device RecallMedical FacilitiesReturn Goods AuthorizationTeleflex Customer

Teleflex and Arrow International Recall ARROW Endurance Extended Dwell Peripheral Catheter System

Published: June 27, 2023

Teleflex and Arrow International recall ARROW Endurance Extended Dwell peripheral catheter system due to risk of catheter separation and leakage

Source: dicardiology.com

Related Topics:

Harrow InternationalTeleflex Customer ServiceCustomer ServiceArrow International Customer ServiceTeleflex Arrow InternationalDrug AdministrationExtended Dwell Peripheral Catheter SystemExtended Dwell Peripheral CatheterRecall DatabaseUrgent Medical Device RecallReturn Goods AuthorizationTeleflex Customer