Teva Pharmaceuticals USA recalls Adrucil (fluorouracil injection, USP) Pharmacy Bulk Package Not for Direct Infusion, 5 g/100 mL (50 mg/mL), For
Presence of Particulate Matter: Black particulate matter was identified as aggregate of silicone rubber pieces from a filler diaphragm and fluorouracil crystals.
Recall notice
Presence of Particulate Matter: Black particulate matter was identified as aggregate of silicone rubber pieces from a filler diaphragm and fluorouracil crystals.
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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/44724-teva-pharmaceuticals-usa-recalls-adrucil-fluorouracil-injection-usp-pharmacy-bulk · Recall date April 28, 2015 · FDA enforcement record: FDA #D-1089-2015
Cite this page
“Teva Pharmaceuticals USA recalls Adrucil (fluorouracil injection, USP) Pharmacy Bulk Package Not for Direct Infusion, 5 g/100 mL (50 mg/mL), For.” GovInfoNow, recall dated April 28, 2015. https://govinfonow.com/recall/44724-teva-pharmaceuticals-usa-recalls-adrucil-fluorouracil-injection-usp-pharmacy-bulk. Based on FDA recall #D-1089-2015 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1089-2015%22&limit=1).
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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-1089-2015 — Teva Pharmaceuticals USA Teva Pharmaceuticals USA recalls Adrucil (fluorouracil injection, USP) Pha Hello, I own a Teva Pharmaceuticals USA recalls Adrucil (fluorouracil injection, USP) Pharmacy Bulk Package Not for Direct Infusion, 5 g/100 mL (50 mg/mL), For that is covered by recall D-1089-2015 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-1089-2015 (April 28, 2015) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-1089-2015 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.
