Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
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FDA Drug Recalls

164 recalls, newest first

Class II · Moderate risk

Zantac 75 mg

CGMP Deviations: Presence of NDMA impurity detected in product.

Ongoing Nitrosamine impurity Sanofi-Aventis U.S. LLC D-0545-2020
Class II · Moderate risk

Zantac 150 mg

CGMP Deviations: Presence of NDMA impurity detected in product.

Ongoing Nitrosamine impurity Sanofi-Aventis U.S. LLC D-0544-2020
Class II · Moderate risk

Ranitidine Tablets

CGMP Deviations: Presence of NDMA impurity detected in product.

Completed Nitrosamine impurity Dr. Reddy's Laboratories, Inc. D-0185-2020
Class II · Moderate risk

Ranitidine Tablets

CGMP Deviations: Presence of NDMA impurity detected in product.

Completed Nitrosamine impurity Dr. Reddy's Laboratories, Inc. NDC 63868-480-24 D-0184-2020
Class II · Moderate risk

Ranitidine Tablets

CGMP Deviations: Presence of NDMA impurity detected in product.

Completed Nitrosamine impurity Dr. Reddy's Laboratories, Inc. NDC 0363-0131-30 D-0183-2020
Class II · Moderate risk

Ranitidine Tablets

CGMP Deviations: Presence of NDMA impurity detected in product.

Completed Nitrosamine impurity Dr. Reddy's Laboratories, Inc. NDC 11673-849-40 D-0179-2020
Class II · Moderate risk

Ranitidine Tablets

CGMP Deviations: Presence of NDMA impurity detected in product.

Completed Nitrosamine impurity Dr. Reddy's Laboratories, Inc. D-0178-2020
Class II · Moderate risk

Ranitidine Tablets

CGMP Deviations: Presence of NDMA impurity detected in product.

Completed Nitrosamine impurity Dr. Reddy's Laboratories, Inc. NDC 71713-203-02 D-0177-2020

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