bioMerieux, Inc. VIDAS Varicella Zoster IgG (VZG) antibody IVD, kit Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
VIDAS Varicella Zoster IgG (VZG) antibody IVD, kit
Brand
bioMerieux, Inc.
Lot Codes / Batch Numbers
US Model 30217-01 Lot 1007410330 and 1007393380
Products Sold
US Model 30217-01 Lot 1007410330 and 1007393380
bioMerieux, Inc. is recalling VIDAS Varicella Zoster IgG (VZG) antibody IVD, kit due to 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 cali. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
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.
Recommended Action
Per FDA guidance
Users are instructed via customer letter to stop using the VIDAS VZG batches 1007410330 and 1007393380 and destroy the remaining products.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026