Class II — Potential Health Hazard

Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.

Meridian Bioscience Recalled by Meridian Bioscience Inc Due to The cap on the reaction buffer tube may...

Date: October 7, 2025
Company: Meridian Bioscience Inc
Status: Ongoing
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 Meridian Bioscience Inc directly.

Affected Products

Meridian Bioscience, Group B Streptococcus, Catalog Number 480050, Nucleic Acid Amplification Test Assay

Quantity: 109 in total

Why Was This Recalled?

The cap on the reaction buffer tube may be missing the black rubber gasket resulting in the potential for leakage and reduced buffer volume.

Where Was This Sold?

This product was distributed to 14 states: AL, CO, FL, GA, IL, ME, MD, MT, NH, NJ, OH, TN, TX, WA

Affected (14 states)Not affected

About Meridian Bioscience Inc

Meridian Bioscience Inc has 15 total recalls tracked by RecallDetector.

Related Recalls

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