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Windstone Medical Packaging, Inc. recalls AMS 4675 Angio Pack. For use in a general clinical procedure.
Recalled December 16, 2015 · FDA recall Z-0377-2016 · Windstone Medical Packaging
Hazard
AMS 4675 Angio Pack is recalled because this kit containing U-SDN 2 Part Ultra Modified Seldinger Needle which is recalled by supplier. · FDA Class II
Units
40 kits
Sold at
Distributed in AL and VA.
Description
AMS 4675 Angio Pack is recalled because this kit containing U-SDN 2 Part Ultra Modified Seldinger Needle which is recalled by supplier.
Product
AMS 4675 Angio Pack. For use in a general clinical procedure.
Manufacturer(s)
Windstone Medical Packaging, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →