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FDAFebruary 20, 2020device

Avalon Elite Vascular Access Kit, Model No. 70106.3540, UDI 04037691831039

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

The hazard

A lot of Avalon Elite Vascular Access Kits (VAK) are being recalled due to a material mix-up with the needle portion of the kit; 81 of 255 kits were assembled with an incorrect Arterial Access Needle instead of a Multi-Purpose Procedure Needle.

What to do

FDA enforcement status: Terminated

Brands named

maquet cardiovascular us salesmaquetmaquet cardiovascular

UPCs

04037691831039

Recall history

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

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