Apotex recalls Rite Aid's Maximum Strength Ranitidine Tablets due to possible contamination with N-nitrosodimethylamine (NDMA).
GGMP Deviations: Possible contamination with impurity N-nitrosodimethylamine (NDMA).
Apotex has recalled Rite Aid's Maximum Strength Ranitidine Tablets (150 mg Cool Mint, 24 tablets) because they may contain a harmful impurity called NDMA. This recall affects consumers who have purchased these tablets from Rite Aid pharmacies.
The tablets may contain N-nitrosodimethylamine (NDMA), a chemical that has been linked to liver damage when consumed in high amounts. While the exact risk level isn't specified in the recall, this impurity is considered a potential health hazard.
Anyone who owns or uses Rite Aid's Maximum Strength Ranitidine Tablets (150 mg Cool Mint, 24 tablets) is affected. People taking these tablets for acid reflux or ulcers are most at risk.
Check for the product name: Rite Aid Pharmacy Maximum Strength Ranitidine Tablets, USP 150 mg Cool Mint Acid Reducer 24 Tablets Sugar Free. The NDC code is 11822-6107-4. These tablets were distributed by Rite Aid in Pennsylvania.
Look for the NDC code 11822-6107-4 on the tablet packaging to confirm if it's part of the recall.
The recall states there is a possible contamination with NDMA, but the exact risk level isn't specified. The manufacturer recommends checking if you have the recalled product.
The recall record does not mention any remedy for refunds or replacements.
The recall indicates a possible contamination with NDMA, which has been linked to liver damage, but the exact risk level isn't specified in the official notice.
We’ve drafted a message you can send Apotex to request your refund or repair — edit it as you like.
Subject: Recall D-0317-2020 — Apotex Apotex Hello, I own a Apotex that is covered by recall D-0317-2020 from Apotex. 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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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.
