FDAClass IIDecember 27, 2023

ZEUS ELISA Parvovirus B19 IgG Test System recall

ZEUS ELISA Parvovirus B19 IgG Test System, Product Number SM9Z7701M

Why was ZEUS ELISA Parvovirus B19 IgG Test System 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.

What should I do if I have this product?

The recall is ongoing. Follow the firm and FDA instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

UDI: (01)00845533001748(17)240731(10)23030068 (01)00845533001755(17)241130(10)23060217 (01)00845533001779(17)241130(10)23060218; Lot Numbers: 23030068 23060217 23060218

Product
ZEUS ELISA Parvovirus B19 IgG Test System, Product Number SM9Z7701M
Recalling firm
Zeus Scientific, Inc.
Quantity
296 kits
Distribution
US States: CA, MA, MI, NJ, NY, TN, UT.
Recall date
December 27, 2023
Classification
Class II
Status
Ongoing
Agency
FDA (device)
Open FDA enforcement record Latest recalls