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Drug recall · FDA · Published August 18, 2017

Zydus Pharmaceuticals USA Inc recalls Paroxetine tablets USP, 30mg, 30-count bottles, Rx Only, Manufactured by: Cadila Healthcare Ltd, Ahmedabad, India

Presence of Foreign tablets/capsules: risperidone Tablets were found in bottle of paroxetine Tablets

🇺🇸 FDA recall #D-1137-2017DrugZydus Pharmaceuticals (USA) Inc ›
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Recalling firmZydus Pharmaceuticals USA Inc73 Route 31 N, N/A · Pennington, NJ 08534-3601
No email on file for this recall — reach the company by phone or its official page instead.No email on file — write to the address above instead.
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Source Page by GovInfoNow · govinfonow.com/recall/41371-zydus-pharmaceuticals-usa-inc-recalls-paroxetine-tablets-usp-30mg-30 · Recall date August 18, 2017 · FDA enforcement record: FDA #D-1137-2017

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“Zydus Pharmaceuticals USA Inc recalls Paroxetine tablets USP, 30mg, 30-count bottles, Rx Only, Manufactured by: Cadila Healthcare Ltd, Ahmedabad, India.” GovInfoNow, recall dated August 18, 2017. https://govinfonow.com/recall/41371-zydus-pharmaceuticals-usa-inc-recalls-paroxetine-tablets-usp-30mg-30. Based on FDA recall #D-1137-2017 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1137-2017%22&limit=1).

How to tell if you have this one

  • Brand
    Zydus Pharmaceuticals (USA) Inc
  • Product
    Zydus Pharmaceuticals USA Inc recalls Paroxetine tablets USP, 30mg, 30-count bottles, Rx Only, Manufactured by: Cadila Healthcare Ltd, Ahmedabad, India
  • Category
    Drug
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Contact Zydus Pharmaceuticals (USA) Inc

We’ve drafted a message you can send Zydus Pharmaceuticals (USA) Inc to request your refund or repair — edit it as you like.

Subject: Recall D-1137-2017 — Zydus Pharmaceuticals (USA) Inc Zydus Pharmaceuticals USA Inc recalls Paroxetine tablets USP, 30mg,

Hello,

I own a Zydus Pharmaceuticals USA Inc recalls Paroxetine tablets USP, 30mg, 30-count bottles, Rx Only, Manufactured by: Cadila Healthcare Ltd, Ahmedabad, India that is covered by recall D-1137-2017 from Zydus Pharmaceuticals (USA) Inc.

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-1137-2017 (August 18, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-1137-2017 to see it in context.
  • 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.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA