Arrow International Inc recalls Catheter, Intravascular, Therapeutic, Long Term Greater than 30 days. An access kit only, contains no base components

Recalled September 21, 2016 · FDA recall Z-2771-2016 · 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, Intravascular, Therapeutic, Long Term Greater than 30 days. An access kit only, contains no base components

Manufacturer(s)

Arrow International Inc

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →