Diamedix Corporation: Medical Device Recall in 2018 - (Recall #: Z-2573-2018)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2018.

Data Source: FDA.

Product Description:

Diamedix Is-Mumps IgG Enzyme Immunoassay Test Kit for In Vitro Diagnostic Use Catalog No. 720-540

Product Classification:

Class III

Date Initiated: January 5, 2018

Date Posted: August 8, 2018

Recall Number: Z-2573-2018

Event ID: 80441

Reason for Recall:

Contains a gel-like contaminant that may affect product performance.

Status: Terminated

Product Quantity: 505

Code Information:

Lot S0406 Exp. 05/31/2018

Distribution Pattern:

AZ, CA, FL, IL, IN, KY, MA, MI, MN, MO, NH, NJ, NY, OH, OK, PA, RI, TN, TX, and WI

Voluntary or Mandated:

Voluntary: Firm initiated