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.

Rite Aid Pharmacy Maximum Strength Ranitidine Tablets Recalled by Apotex Inc. Due to GGMP Deviations: Possible contamination with impurity N-nitrosodimethylamine (NDMA).

Date: September 24, 2019
Company: Apotex Inc.
Status: Completed
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 Apotex Inc. directly.

Affected Products

Rite Aid Pharmacy Maximum Strength Ranitidine Tablets, USP 150 mg Cool Mint Acid Reducer 24 Tablets Sugar Free NDC 11822-6107-4 Distributed By: Rite Aid 30 Hunter Lane, Camp Hill, PA 17011

Quantity: 31,968 bottles

Why Was This Recalled?

GGMP Deviations: Possible contamination with impurity N-nitrosodimethylamine (NDMA).

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Apotex Inc.

Apotex Inc. has 41 total recalls tracked by RecallDetector.

Related Recalls

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