Infusion Options recalls 8mg/50ml ONDANSETRON IV solutions for lack of sterility assurance. All lots within expiry date are affected. Consumers should contact the company for details.
Lack of Assurance of Sterility
Infusion Options is recalling all 8 mg/50 ml ONDANSETRON IV solutions because they may not be sterile. This could lead to infections if used improperly.
The product lacks assurance of sterility, meaning it might contain harmful bacteria or contaminants. If used, this could cause infections or other health issues.
Patients receiving IV medication from this product are affected. Healthcare providers using the product for medical treatments are at risk.
Check for the product name 'ONDANSETRON 8 MG / 50 ml NS IVPB' on the label. All lots within the expiry date are affected.
Reach out to Infusion Options, Inc. at 718-283-7233 for specific product details and instructions.
The recall states there is a lack of assurance of sterility, so it may not be safe. Consult the manufacturer for details.
Look for the product name 'ONDANSETRON 8 MG / 50 ml NS IVPB' on the label. All lots within the expiry date are affected.
Contact Infusion Options, Inc. at 718-283-7233 for specific instructions on what to do with the product.
We’ve drafted a message you can send Infusion Options to request your refund or repair — edit it as you like.
Subject: Recall D-1794-2019 — Infusion Options Infusion Options Hello, I own a Infusion Options that is covered by recall D-1794-2019 from Infusion Options. 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.
