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Arrow International Inc recalls Multi-Lumen Central Venous Catheterization Kit
Recalled October 22, 2014 · FDA recall Z-0076-2015 · Arrow International
Hazard
Arrow International, Inc. has initiated a voluntary recall for product code AK- 12703, lot number RF3039028 because the label on the outer corrugate is labeled with the incorrect expiration date. All kits packaged within the corrugate are correctly labeled. There is no risk to the patient as the kits within the corrugate are labeled with the correct expiration date. · FDA Class II
Units
65
Sold at
US Distribution including the states of MD, NC , LA , IN , OH, KY, CA , PA , NY and NV.
Description
Arrow International, Inc. has initiated a voluntary recall for product code AK- 12703, lot number RF3039028 because the label on the outer corrugate is labeled with the incorrect expiration date. All kits packaged within the corrugate are correctly labeled. There is no risk to the patient as the kits within the corrugate are labeled with the correct expiration date.
Product
Multi-Lumen Central Venous Catheterization Kit
Manufacturer(s)
Arrow International Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →