FDAAugust 1, 2017device

Presource(R) Kits (custom surgical/procedural kits): The standard and custom kits are packed with all of the specific disposable class I, II, and II implantable, life-supporting, or life-sustaining devices required by customers for common surgical and other medical procedures

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

The hazard

The firm manufactured and distributed Presource(R) kits which contained BD SafetyGlide" 22GA 1¿ inch Needles. BD subsequently recalled these needles because, " Loose polypropylene particulate in the fluid path could be expelled out of the needle during injection.

What to do

FDA enforcement status: Terminated

Brands named

cardinal health 200cardinalcardinal health

UPCs

262503485950262503604487262503643270262503673080262927407083262927416194317479378307317479380125319456380294319456414203

Recall history

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

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