FDANovember 2, 2015device

AMS 4674 Custom Pack. For use in a general clinical procedure.

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

AMS 4674 Custom Pack is recalled because this kit containing U-SDN 2 Part Ultra Modified Seldinger Needle which is recalled by supplier.

What to do

FDA enforcement status: Terminated

Brands named

windstone medical packagingwindstonewindstone medical

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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AMS 4674 Custom Pack. For use in a general clinical procedure. — Recall Details · AllClear