FDA recall record

bioMerieux VIDAS CMV IgM, 30 tests, REF 30205-01, IVD, Rx recall — FDA Z-0742-2022

Invalid calibrations (out of range high) while using the product.

Class IIclassification
Z-0742-2022official record ID
Oct 5, 2022report date

Recall record at a glance

Official recordZ-0742-2022
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmbioMerieux, Inc.
Report dateOct 5, 2022
Recall initiation dateFeb 9, 2022
Quantity480 kits
LocationDurham, NC, United States

Official product description

VIDAS CMV IgM, 30 tests, REF 30205-01, IVD, Rx.

Why the product was recalled

Invalid calibrations (out of range high) while using the product.

Distribution information

Distribution was made to CA, FL, GA, IL, IN, LA, MA, MD, ME, MO, NJ, NY, OH, PA, TX, VA, WI, and WV. There was government distribution but no military or foreign distribution.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

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