Skip to content
Recall Observatory FDA recall evidence

Device product

ZEUS ELISA Parvovirus B19 IgM Test System, UDI 00845533001755 - Product Usage: intended for the qualitative detection of IgM class antibodies to human Parvovirus B19 in human serum including women of childbearing age where there is a suspicion of exposure to human Parvovirus B19.

Z-3026-2020

August 12, 2019

Class II

Product summary

Firm
Zeus Scientific, Inc.
Event
Event 86364
Status
Terminated
Classification
Class II
Quantity
74
Official record key
device-enforcement:Z-3026-2020

Official wording

Reason: FDA inspection identified that due to increased positivity (false positives) on the Parvovirus B19 ELISA Test System, the firm assigned a new Correction Factor and new lot number to the remainder of the affected lot, and distributed the reworked product to the customer.

Code information: Lot 19040014

Distribution pattern: Worldwide distribution - US Nationwide distribution including in the states of CA, CT, IN, NJ, TX and the country of Canada.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    FDA inspection identified that due to increased positivity (false positives) on the Parvovirus B19 ELISA Test System, the firm assigned a new Correction Factor and new lot number to the remainder of the affected lot, and distributed the reworked product to the customer.