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Arrow International Inc recalls Radial Artery Catheterization Set, 1) NA-04550-1A & 2) NA-04550-X1A, device permits access to the peripheral arterial ci
Recalled February 21, 2018 · FDA recall Z-0486-2018 · Arrow International
Hazard
Needle supplier indicated the presence of loose polypropylene foreign matter above release specification. · FDA Class II
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Description
Needle supplier indicated the presence of loose polypropylene foreign matter above release specification.
Product
Radial Artery Catheterization Set, 1) NA-04550-1A & 2) NA-04550-X1A, device permits access to the peripheral arterial circulation or to other small vessels.
Manufacturer(s)
Arrow International Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →