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Drug recall · FDA · Published July 24, 2015

Teva Pharmaceuticals USA recalls ADRUCIL (fluorouracil injection, USP), 5 g/100 mL (50 mg/mL) glass vials, 5 x 100 ml vials per carton, manufactured by

Presence of Particulate Matter: silcone rubber and fluorouracil crystals found floating in solution

🇺🇸 FDA recall #D-1351-2015DrugTeva Pharmaceuticals USA ›
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Recalling firmTeva Pharmaceuticals USA425 Privet Rd, N/A · Horsham, PA 19044-1220
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/43976-teva-pharmaceuticals-usa-recalls-adrucil-fluorouracil-injection-usp-5-g · Recall date July 24, 2015 · FDA enforcement record: FDA #D-1351-2015

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“Teva Pharmaceuticals USA recalls ADRUCIL (fluorouracil injection, USP), 5 g/100 mL (50 mg/mL) glass vials, 5 x 100 ml vials per carton, manufactured by.” GovInfoNow, recall dated July 24, 2015. https://govinfonow.com/recall/43976-teva-pharmaceuticals-usa-recalls-adrucil-fluorouracil-injection-usp-5-g. Based on FDA recall #D-1351-2015 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1351-2015%22&limit=1).

How to tell if you have this one

  • 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-1351-2015 — Teva Pharmaceuticals USA Teva Pharmaceuticals USA recalls ADRUCIL (fluorouracil injection, USP), 5 

Hello,

I own a Teva Pharmaceuticals USA recalls ADRUCIL (fluorouracil injection, USP), 5 g/100 mL (50 mg/mL) glass vials, 5 x 100 ml vials per carton, manufactured by that is covered by recall D-1351-2015 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-1351-2015 (July 24, 2015) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-1351-2015 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