PlainRecalls
FDA Devices Moderate Class II Ongoing

Parvovirus B19 IgG EIA kit Part No. V519IGUS

Reported: September 9, 2020 Initiated: July 17, 2020 #Z-2936-2020

Product Description

Parvovirus B19 IgG EIA kit Part No. V519IGUS

Reason for Recall

Printed label inside the box lid of the Parvovirus has the incorrect Lot Specific Constant value

Details

Recalling Firm
Diasorin Inc.
Units Affected
615 units
Distribution
NJ, WI, NY, NC, MN, CA, IL, VA, MA, MI, CT Canada
Location
Stillwater, MN

Frequently Asked Questions

What product was recalled?
Parvovirus B19 IgG EIA kit Part No. V519IGUS. Recalled by Diasorin Inc.. Units affected: 615 units.
Why was this product recalled?
Printed label inside the box lid of the Parvovirus has the incorrect Lot Specific Constant value
Which agency issued this recall?
This recall was issued by the FDA Devices on September 9, 2020. Severity: Moderate. Recall number: Z-2936-2020.