Ranitidine is a heartburn medication withdrawn from the market over NDMA contamination concerns. We track every FDA enforcement recall involving Ranitidine (Zantac) — 7 recalls in our database, including 3 active.
Add Ranitidine to your medicine cabinet and we’ll email you the moment the FDA issues a new recall — before your pharmacy calls. Free forever, no credit card.
Granules India Limited — CGMP Deviations: Impurity N-nitrosodimethylamine (NDMA) found in API
Recall D-0632-2020
Amneal Pharmaceuticals, Inc. — CGMP Deviations: Impurity N-nitrosodimethylamine (NDMA) found in API
Recall D-0616-2020
Amneal Pharmaceuticals, Inc. — CGMP Deviations: Impurity N-nitrosodimethylamine (NDMA) found in API
Recall D-0615-2020
Dr. Reddy's Laboratories, Inc. — CGMP Deviations: Presence of NDMA impurity detected in product.
Recall D-0181-2020
Dr. Reddy's Laboratories, Inc. — CGMP Deviations: Presence of NDMA impurity detected in product.
Recall D-0182-2020
Dr. Reddy's Laboratories, Inc. — CGMP Deviations: Presence of NDMA impurity detected in product.
Recall D-0168-2020
Dr. Reddy's Laboratories, Inc. — CGMP Deviations: Presence of NDMA impurity detected in product.
Recall D-0180-2020
This page is for information only and isn’t medical advice. Always follow your clinician’s guidance.
The FDA publishes recalls, but most never make the news. The reliable way is an automated alert: sign up free and we’ll email you when a Ranitidine recall is issued.
Most prescriptions filled in the US are generics, so most recalls involve generic products. A recall doesn’t mean the drug itself is unsafe — it usually affects specific lots or manufacturers.
Yes — weekly recall alert digests are free forever, with no credit card required. See pricing.