FDA recall record

ZEUS ELISA Parvovirus B19 IgG Test System, Product Number SM9Z7701M recall — FDA Z-0602-2024

The organization completed a product improvement process to the conjugate found within the certain ELISA kits. This modification was not reviewed and…

Class IIclassification
Z-0602-2024official record ID
Dec 27, 2023report date

Recall record at a glance

Official recordZ-0602-2024
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmZeus Scientific, Inc.
Report dateDec 27, 2023
Recall initiation dateOct 31, 2023
Quantity296 kits
LocationBranchburg, NJ, United States

Official product description

ZEUS ELISA Parvovirus B19 IgG Test System, Product Number SM9Z7701M

Why the product was recalled

The organization completed a product improvement process to the conjugate found within the certain ELISA kits. This modification was not reviewed and approved by FDA prior to its implementation.

Distribution information

US States: CA, MA, MI, NJ, NY, TN, UT.

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

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