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Drug recall · FDA · Published November 6, 2017

Claris Lifesciences Inc recalls Ciprofloxacin in Dextrose (5%) Injection, USP 200 mg in 100 mL 5% Dextrose, Rx Only, (2 mg/mL), 100 mL Flexible Bag,

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🇺🇸 FDA recall #D-0127-2018DrugClaris Lifesciences Inc ›
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Recalling firmClaris Lifesciences Inc1445 US Highway 130 · North Brunswick, NJ 08902-3100
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/41106-claris-lifesciences-inc-recalls-ciprofloxacin-in-dextrose-5-injection-usp · Recall date November 6, 2017 · FDA enforcement record: FDA #D-0127-2018

Cite this page

“Claris Lifesciences Inc recalls Ciprofloxacin in Dextrose (5%) Injection, USP 200 mg in 100 mL 5% Dextrose, Rx Only, (2 mg/mL), 100 mL Flexible Bag,.” GovInfoNow, recall dated November 6, 2017. https://govinfonow.com/recall/41106-claris-lifesciences-inc-recalls-ciprofloxacin-in-dextrose-5-injection-usp. Based on FDA recall #D-0127-2018 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0127-2018%22&limit=1).

How to tell if you have this one

  • Brand
    Claris Lifesciences Inc
  • Product
    Ciprofloxacin in Dextrose (5%) Injection, USP 200 mg in 100 mL 5% Dextrose, Rx Only, (2 mg/mL), 100 mL Flexible Bag
  • Category
    Drug
Take action

Contact Claris Lifesciences Inc

We’ve drafted a message you can send Claris Lifesciences Inc to request your refund or repair — edit it as you like.

Subject: Recall D-0127-2018 — Claris Lifesciences Inc Ciprofloxacin in Dextrose (5%) Injection, USP 200 mg in 100 mL 5% Dextrose,

Hello,

I own a Ciprofloxacin in Dextrose (5%) Injection, USP 200 mg in 100 mL 5% Dextrose, Rx Only, (2 mg/mL), 100 mL Flexible Bag that is covered by recall D-0127-2018 from Claris Lifesciences 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-0127-2018 (November 6, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0127-2018 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