Class III — Low Risk

Low risk — use of or exposure to this product is not likely to cause adverse health consequences.

Diamedix Is-Mumps IgG Enzyme Immunoassay Test Kit for In Vitro Recalled by Diamedix Corporation Due to Contains a gel-like contaminant that may affect product...

Date: January 5, 2018
Company: Diamedix Corporation
Status: Terminated
Source: FDA (Device)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact Diamedix Corporation directly.

Affected Products

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

Quantity: 505

Why Was This Recalled?

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

Where Was This Sold?

This product was distributed to 20 states: AZ, CA, FL, IL, IN, KY, MA, MI, MN, MO, NH, NJ, NY, OH, OK, PA, RI, TN, TX, WI

Affected (20 states)Not affected

About Diamedix Corporation

Diamedix Corporation has 7 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Device). Last updated March 26, 2026. View original report