Baxter Healthcare Corporation is recalling approximately 13,000 containers of Acetaminophen Injection (1000 mg/100 mL). The product, which is a prescription medication administered in medical settings, is being recalled because the solution may be discolored. The recall affects 100 mL Viaflo containers from lot 24A27G66.
Discoloration in an intravenous medication can indicate that the drug has degraded or been contaminated. Administering a discolored or degraded medication could cause unexpected side effects or lead to the patient not receiving the proper dose of the medicine.
Rx only; Manufactured in Ireland for Baxter Healthcare Corporation.
If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.
This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.
AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.
Sources: FDA iRES · Raw API Response
openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.