Sanofi Zantac 150mg Recall: NDMA Impurity Risk

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Contact the company & request your remedy

Recalling firmSanofi-Aventis U.S. LLC55 Corporate Dr · Bridgewater, NJ 08807-1265

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✎ GovInfoNow plain-language explainer

What happened, in plain English

Sanofi is recalling all lots of Zantac 150mg tablets after finding NDMA impurities. This chemical has been linked to potential health risks, so affected consumers should stop using the product and contact Sanofi for guidance.

Why it’s dangerous

NDMA is a chemical that has been found in some medications and has been linked to potential health risks, including liver damage. The presence of this impurity in Zantac 150mg tablets is a concern because it can be harmful to consumers.

Who’s affected

All owners of Zantac 150mg tablets distributed by Sanofi are affected. People taking this medication for heartburn or ulcers are most at risk.

How to tell if you have this one

Check for Zantac 150mg tablets with NDC code 67751-151-01. All lots of this product are included in the recall.

Brand
Sanofi
Category
Drug

Based on the official FDA remedy

What to do — step by step

Stop Using It Now
Immediately stop using Zantac 150mg tablets and contact Sanofi for instructions.

✎ GovInfoNow

Questions people ask

Is this recall affecting all Zantac 150mg tablets?

Yes, all lots of Zantac 150mg tablets distributed by Sanofi are affected.

What should I do if I have Zantac 150mg tablets?

Stop using them immediately and contact Sanofi for guidance.

Is there a risk of serious injury from this product?

The recall is due to NDMA impurities, which have been linked to potential health risks, but the official notice does not specify a risk of serious injury.

Take action

Contact Sanofi

We’ve drafted a message you can send Sanofi to request your refund or repair — edit it as you like.

✉️ Open in email

Subject: Recall D-0541-2020 — Sanofi Sanofi

Hello,

I own a Sanofi that is covered by recall D-0541-2020 from Sanofi.

I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this?

Thank you.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

Official source: FDA Recall #D-0541-2020 (October 22, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0541-2020 to see it in context.
Plain-language summary written by qwen3:4b on August 18, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.

Sanofi-Aventis U.S. LLC recalls Regular Strength Zantac 150 mg, Distributed by: Chattem, Inc., a Sanofi Company P.O. Box 2219, Chattanooga, TN

Recall notice