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Drug recall · FDA · Published July 6, 2017

Baxter Healthcare Corporation recalls 0.9% Sodium Chloride Injection USP, 250 mL VIAFLEX Container bag, Rx only, Baxter Healthcare Corporation, Deerfield, IL

Lack of Assurance of Sterility: Customer complaints for leaking bags.

🇺🇸 FDA recall #D-0957-2017DrugBaxter Healthcare Corporation ›
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Recalling firmBaxter Healthcare Corporation1 Baxter Pkwy · Deerfield, IL 60015-4625
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/41511-baxter-healthcare-corporation-recalls-0-9-sodium-chloride-injection-usp · Recall date July 6, 2017 · FDA enforcement record: FDA #D-0957-2017

Cite this page

“Baxter Healthcare Corporation recalls 0.9% Sodium Chloride Injection USP, 250 mL VIAFLEX Container bag, Rx only, Baxter Healthcare Corporation, Deerfield, IL.” GovInfoNow, recall dated July 6, 2017. https://govinfonow.com/recall/41511-baxter-healthcare-corporation-recalls-0-9-sodium-chloride-injection-usp. Based on FDA recall #D-0957-2017 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0957-2017%22&limit=1).

How to tell if you have this one

  • Brand
    Baxter Healthcare Corporation
  • Category
    Drug
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Contact Baxter Healthcare Corporation

We’ve drafted a message you can send Baxter Healthcare Corporation to request your refund or repair — edit it as you like.

Subject: Recall D-0957-2017 — Baxter Healthcare Corporation Baxter Healthcare Corporation recalls 0.9% Sodium Chloride Injection 

Hello,

I own a Baxter Healthcare Corporation recalls 0.9% Sodium Chloride Injection USP, 250 mL VIAFLEX Container bag, Rx only, Baxter Healthcare Corporation, Deerfield, IL that is covered by recall D-0957-2017 from Baxter Healthcare Corporation.

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-0957-2017 (July 6, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0957-2017 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