FDAMarch 3, 2017device

The CG+ Arrow PIC Catheters permit venous access to the central circulation through a peripheral vein.

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

The hazard

Arrow International, Inc. notified its customers who received the affected Antimicrobial/Antithrombogenic PICC Kits, that the kits were being recalled due to a labeling error. The lidstock on some of the kits reads CDC-45541-HPK1A, while the banner card on the side of the kit reads CDC-45052-HPK1A. Other kits may list CDC-45052-HPK1A on the lidstock and CDC-45541-HPK1A on the banner card. The affected lot numbers are 23F16C0851, 23F16A0727, and 23F16C0844.

What to do

FDA enforcement status: Terminated

Brands named

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Recall history

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

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The CG+ Arrow PIC Catheters permit venous access to the central circulation through a peripheral vein. — Recall Details · AllClear