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Drug recall · FDA · Published February 5, 2016

Teva Pharmaceuticals USA recalls Paricalcitol Capsules, 1 mcg, 30 tablets per Bottle, Rx Only, Manufactured By: Pharmaceutics International, Inc., Hunt

Failed Impurities/Degradation Specifications: Out of specification test results for impurities during stability testing.

🇺🇸 FDA recall #D-0774-2016DrugTeva Pharmaceuticals USA ›
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Recalling firmTeva Pharmaceuticals USA1090 Horsham Rd · North Wales, PA 19454-1505
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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We break every recall down into plain English — this one’s still on our list. Until our write-up is ready, the official FDA hazard and remedy below have the full, accurate details.

Source Page by GovInfoNow · govinfonow.com/recall/43170-teva-pharmaceuticals-usa-recalls-paricalcitol-capsules-1-mcg-30-tablets · Recall date February 5, 2016 · FDA enforcement record: FDA #D-0774-2016

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“Teva Pharmaceuticals USA recalls Paricalcitol Capsules, 1 mcg, 30 tablets per Bottle, Rx Only, Manufactured By: Pharmaceutics International, Inc., Hunt.” GovInfoNow, recall dated February 5, 2016. https://govinfonow.com/recall/43170-teva-pharmaceuticals-usa-recalls-paricalcitol-capsules-1-mcg-30-tablets. Based on FDA recall #D-0774-2016 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0774-2016%22&limit=1).

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  • Brand
    Teva Pharmaceuticals USA
  • Category
    Drug
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Contact Teva Pharmaceuticals USA

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

Subject: Recall D-0774-2016 — Teva Pharmaceuticals USA Teva Pharmaceuticals USA recalls Paricalcitol Capsules, 1 mcg, 30 tablets 

Hello,

I own a Teva Pharmaceuticals USA recalls Paricalcitol Capsules, 1 mcg, 30 tablets per Bottle, Rx Only, Manufactured By: Pharmaceutics International, Inc., Hunt that is covered by recall D-0774-2016 from Teva Pharmaceuticals USA.

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-0774-2016 (February 5, 2016) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0774-2016 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