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Arrow International Inc recalls Radial Artery Catheterization Kit; Model: AK-04220
Recalled April 11, 2018 · FDA recall Z-1286-2018 · 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
6358
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
Radial Artery Catheterization Kit; Model: AK-04220
Manufacturer(s)
Arrow International Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →