Zydus Pharmaceuticals recalls 75mg Venlafaxine tablets due to foreign material found in one tablet. This is a prescription-only product with specific lot numbers and expiration dates.
Presence of Foreign Substance: Product complaint received for the presence of foreign material embedded resembling a metal shaving in one tablet.
Zydus Pharmaceuticals is recalling 75mg Venlafaxine tablets after reports of foreign material in one tablet. This is a prescription-only medication that could pose a risk if the foreign substance causes injury during use.
The product complaint reports a foreign material resembling a metal shaving found in one tablet. This could potentially cause injury if the material cuts or irritates the mouth or throat during ingestion.
Prescription patients who have the specific lot number (M314265) of Venlafaxine 75mg tablets. Those with the product from the manufacturer in Ahmedabad, India, are most at risk.
Check for the lot number M314265 on the packaging. The product is a prescription-only medication with an expiration date of October 31, 2025.
Look for the lot number M314265 on the packaging of the Venlafaxine tablets.
The recall is due to a foreign material found in one tablet, but the product is generally safe for most users. Consult your doctor if you have concerns.
Check the lot number on the packaging. If it matches M314265, contact Zydus Pharmaceuticals for guidance.
The recall reports a foreign material in one tablet, but no specific injuries have been reported. The risk is low and not severe.
We’ve drafted a message you can send Zydus Pharmaceuticals to request your refund or repair — edit it as you like.
Subject: Recall D-0310-2025 — Zydus Pharmaceuticals Zydus Pharmaceuticals Hello, I own a Zydus Pharmaceuticals that is covered by recall D-0310-2025 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.
