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Arrow International Inc recalls Catheter, Percutaneous The Arrow Single-Lumen Catheter permits venous access to the central circulation.
Recalled September 21, 2016 · FDA recall Z-2773-2016 · Arrow International
Hazard
Notification of component molding abnormality by supplier used to package certain Arrow Select Kit (ASK) products. · FDA Class II
Units
6,121 units in total
Sold at
US Distribution to states of: NC, OH, FL, and MD.
Description
Notification of component molding abnormality by supplier used to package certain Arrow Select Kit (ASK) products.
Product
Catheter, Percutaneous The Arrow Single-Lumen Catheter permits venous access to the central circulation.
Manufacturer(s)
Arrow International Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →