Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
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Class II · Moderate risk Terminated Initiated May 31, 2019 (7 years ago)

Gericare Geri-Tussin DM

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

cGMP Deviations: Products may have microbial contamination.

Cause type: Microbial contamination

Bacteria, mold, yeast or other microorganisms detected in the product. Contamination can occur from water systems, equipment or handling, and can cause infection. All microbial contamination recalls.

What was recalled

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

Affected NDC 57896-0660-16

Compare with the code on your package — it is the most precise check available.

Recalling firm
Geritrex, LLC
NDC code
57896-660-16
Origin
NY, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1526-2019 · FDA notice

Check, then ask. Class II means harm is possible but usually temporary or reversible. Find the lot number on your package; if it matches, ask your pharmacist about a replacement. Do not simply stop a prescribed medication on your own - the gap can be riskier than the recall. This recall is now terminated, which means the firm has finished removing the affected product; anything on pharmacy shelves today should be unaffected.

Other recalls by Geritrex, LLC

All 2019 recalls

Other microbial contamination recalls from 2019

All microbial contamination recalls