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Drug recall · FDA · Published April 24, 2017

Teva Pharmaceuticals USA recalls Clozapine Tablets USP, 25 mg, 100-count bottle (NDC 0093-4359-01), 500- count bottle (NDC 0093-4359-05), 100 Unit Dose

Microbial Contamination of Non-Sterile Products

🇺🇸 FDA recall #D-0705-2017DrugTeva Pharmaceuticals USA ›
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Recalling firmTeva Pharmaceuticals USA1090 Horsham Rd, N/A · 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/41640-teva-pharmaceuticals-usa-recalls-clozapine-tablets-usp-25-mg-100 · Recall date April 24, 2017 · FDA enforcement record: FDA #D-0705-2017

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“Teva Pharmaceuticals USA recalls Clozapine Tablets USP, 25 mg, 100-count bottle (NDC 0093-4359-01), 500- count bottle (NDC 0093-4359-05), 100 Unit Dose.” GovInfoNow, recall dated April 24, 2017. https://govinfonow.com/recall/41640-teva-pharmaceuticals-usa-recalls-clozapine-tablets-usp-25-mg-100. Based on FDA recall #D-0705-2017 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0705-2017%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-0705-2017 — Teva Pharmaceuticals USA Teva Pharmaceuticals USA recalls Clozapine Tablets USP, 25 mg, 100-count b

Hello,

I own a Teva Pharmaceuticals USA recalls Clozapine Tablets USP, 25 mg, 100-count bottle (NDC 0093-4359-01), 500- count bottle (NDC 0093-4359-05), 100 Unit Dose that is covered by recall D-0705-2017 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-0705-2017 (April 24, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0705-2017 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