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Drug recall · FDA · Published July 6, 2017

Baxter Healthcare Corporation recalls 5% Dextrose Injection, USP, 100 mL VIAFLEX Plastic Container, Rx only, Baxter Healthcare Corporation, Deerfield IL

Lack of Assurance of Sterility: Bags have the potential to leak.

🇺🇸 FDA recall #D-0972-2017DrugBaxter 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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Source Page by GovInfoNow · govinfonow.com/recall/41513-baxter-healthcare-corporation-recalls-5-dextrose-injection-usp-100-ml · Recall date July 6, 2017 · FDA enforcement record: FDA #D-0972-2017

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“Baxter Healthcare Corporation recalls 5% Dextrose Injection, USP, 100 mL VIAFLEX Plastic Container, Rx only, Baxter Healthcare Corporation, Deerfield IL.” GovInfoNow, recall dated July 6, 2017. https://govinfonow.com/recall/41513-baxter-healthcare-corporation-recalls-5-dextrose-injection-usp-100-ml. Based on FDA recall #D-0972-2017 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0972-2017%22&limit=1).

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  • Brand
    Baxter Healthcare Corporation
  • Category
    Drug
FDA recall event · 2 products

All 2 products in this recall

FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.

  • Classification
    Class II
  • Status
    Terminated
  • Distribution
    Nationwide, Puerto Rico and Saudi Arabia
Recall numberProduct, codes & lotsQuantityNDC
D-0972-20175% Dextrose Injection, USP, 100 mL VIAFLEX Plastic Container, Rx only, Baxter Healthcare Corporation, Deerfield IL 60015 USA, Product Code: 2B0089, NDC: 0338-0017-38; Lot: P361618, Exp 09/30/18;54,528 bags0338-0017-10, 0338-0017-41, 0338-0017-11, 0338-0017-31, 0338-0017-48, 0338-0017-18, 0338-0017-38, 0338-0017-02, 0338-0017-03, 0338-0017-04, 0338-0023-02, 0338-0023-03, 0338-0023-04
D-0973-20170.9% Sodium Chloride Injection, USP, 100 mL VIAFLEX Container, Rx Only, Baxter Healthcare Corporation, Deerfield IL 60015 USA, Product Code: 2B1309, NDC: 0338-0049-38; Lots: P361501, P361667, and P361790, Exp 09/30/18295,200 bags0338-0049-01, 0338-0049-02, 0338-0049-03, 0338-0049-04, 0338-0049-10, 0338-0049-41, 0338-0049-11, 0338-0049-31, 0338-0049-48, 0338-0049-18, 0338-0049-38, 0338-0043-03, 0338-0043-04
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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-0972-2017 — Baxter Healthcare Corporation Baxter Healthcare Corporation recalls 5% Dextrose Injection, USP, 100

Hello,

I own a Baxter Healthcare Corporation recalls 5% Dextrose Injection, USP, 100 mL VIAFLEX Plastic Container, Rx only, Baxter Healthcare Corporation, Deerfield IL that is covered by recall D-0972-2017 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-0972-2017 (July 6, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0972-2017 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