Class II โ€” Potential Health Hazard

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

Gericare Geri-Tussin DM Recalled by Geritrex, LLC Due to cGMP Deviations: Products may have microbial contamination.

Date: May 31, 2019
Company: Geritrex, LLC
Status: Terminated
Source: FDA (Drug)

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 Geritrex, LLC directly.

Affected Products

Gericare Geri-Tussin DM, 16 FL OZ (473 mL), Geri-care Phamaceuticals Corp. 1650 63rd Street Brooklyn, NY, NDC 57896-660-16

Quantity: 6213 bottles

Why Was This Recalled?

cGMP Deviations: Products may have microbial contamination.

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Geritrex, LLC

Geritrex, LLC has 10 total recalls tracked by RecallDetector.

Related Recalls

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