Baxter recalls Ondansetron Injection (4 mg/2 mL) due to failed pH specifications. This may affect medication safety. Check NDC 36000-012-25 and lot numbers for affected products.
Failed pH Specifications
Baxter is recalling Ondansetron Injection, 4 mg/2 mL vials, because the product failed pH specifications. This could lead to medication safety issues if used as intended.
The product failed pH specifications, which means the medication may not be stable or effective. This could lead to improper treatment outcomes or safety risks if used without proper pH balance.
Prescription patients using Ondansetron Injection for nausea or vomiting. Healthcare providers administering the medication are most at risk.
Check the NDC code 36000-012-25 and lot numbers listed (e.g., A0E0959A, A0F0533A). Products manufactured in India with specific expiration dates are affected.
Identify the NDC code 36000-012-25 and lot numbers from the list provided in the recall notice.
The recall states the product failed pH specifications, but the official notice does not specify if it is safe to use.
The recall remedy is not stated, so the official notice does not provide specific actions to take.
Check the NDC code 36000-012-25 and lot numbers listed in the recall notice (e.g., A0E0959A, A0F0533A).
We’ve drafted a message you can send Baxter to request your refund or repair — edit it as you like.
Subject: Recall D-0146-2024 — Baxter Baxter Hello, I own a Baxter that is covered by recall D-0146-2024 from Baxter. 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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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.
