FDADecember 10, 2019device

VIDAS Varicella Zoster IgG (VZG) antibody IVD, kit

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

The hazard

Two batches of VIDAS Varicella-Zoster IgG (VZG ref 30217) may yield an invalid calibration which may delay the patient's sample result or a valid calibration may lead to a false positive patient result.

What to do

FDA enforcement status: Terminated

Brands named

biomerieux

Recall history

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

Own something like this?

AllClear screens your whole list against every CPSC, FDA, USDA and NHTSA recall — and tells you the day a new one names something you own.

Start free — 200 items, no card →