Baxter Healthcare Corporation recalls 0.9% Sodium Chloride Injection, USP, 100 mL MINI-BAG VIAFLEX Container, Single Dose Container, Rx Only, Baxter
Lack of Assurance of Sterility: Recalling firm reported a complaint for mold on the interior surface of the overpouch.
Recall notice
Lack of Assurance of Sterility: Recalling firm reported a complaint for mold on the interior surface of the overpouch.
Contact the company & request your remedy
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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/43780-baxter-healthcare-corporation-recalls-0-9-sodium-chloride-injection-usp · Recall date September 2, 2015 · FDA enforcement record: FDA #D-1816-2015
Cite this page
“Baxter Healthcare Corporation recalls 0.9% Sodium Chloride Injection, USP, 100 mL MINI-BAG VIAFLEX Container, Single Dose Container, Rx Only, Baxter.” GovInfoNow, recall dated September 2, 2015. https://govinfonow.com/recall/43780-baxter-healthcare-corporation-recalls-0-9-sodium-chloride-injection-usp. Based on FDA recall #D-1816-2015 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1816-2015%22&limit=1).
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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-1816-2015 — 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, 100 mL MINI-BAG VIAFLEX Container, Single Dose Container, Rx Only, Baxter that is covered by recall D-1816-2015 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-1816-2015 (September 2, 2015) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-1816-2015 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.