Zydus Pharmaceuticals recalls 250mg Erythromycin tablets with potential N-Nitroso-Desmethyl-Erythromycin above safe levels. Rx-only bottles from specific NDCs and lots may pose health risks.
CGMP Deviations; presence of N-Nitroso-Desmethyl-Erythromycin above the recommended acceptable intake limit
Zydus Pharmaceuticals is recalling certain 250mg Erythromycin tablets due to potential presence of N-Nitroso-Desmethyl-Erythromycin above safe limits. This could pose health risks to people using these prescription medications.
The tablets may contain N-Nitroso-Desmethyl-Erythromycin levels exceeding the recommended safe intake. This chemical is linked to potential health risks, though the exact danger level isn't specified in the recall.
Prescription users of the recalled Erythromycin tablets. People with specific NDC numbers and production lots are most at risk.
Check for 250mg Erythromycin tablets with NDC numbers 70710-1047-3 (30-count) or 70710-1047-1 (100-count). Also look for production lots M411146, M502098, M502097 (expiring 08/2026 or 01/2027) or M411145 (expiring 08/2026).
Identify your Erythromycin tablets by NDC number and production lot to confirm if they are recalled.
The recall states there may be N-Nitroso-Desmethyl-Erythromycin above safe levels, but the exact health risk isn't specified. Consult your doctor for advice.
The recall does not provide specific action steps. Check the product details to see if you have the recalled items.
Look for NDC numbers 70710-1047-3 or 70710-1047-1 and production lots M411146, M502098, M502097, or M411145 on the packaging.
We’ve drafted a message you can send Zydus Pharmaceuticals to request your refund or repair — edit it as you like.
Subject: Recall D-0544-2026 — Zydus Pharmaceuticals Zydus Pharmaceuticals Hello, I own a Zydus Pharmaceuticals that is covered by recall D-0544-2026 from Zydus Pharmaceuticals. 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.
