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Arrow International Inc recalls Arterial Access Tray, introducer catheter; Model: GU-04020
Recalled April 11, 2018 · FDA recall Z-1287-2018 · Arrow International
Hazard
The povidone iodine prep pads included in certain kits and trays do not meet the requirements for a 36-month shelf life and should be labeled with a 24-month shelf life. · FDA Class II
Units
1190
Sold at
US nationwide distribution, including Puerto Rico.
Description
The povidone iodine prep pads included in certain kits and trays do not meet the requirements for a 36-month shelf life and should be labeled with a 24-month shelf life.
Product
Arterial Access Tray, introducer catheter; Model: GU-04020
Manufacturer(s)
Arrow International Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →