Baxter Healthcare’s Acetaminophen Injection 1000 mg/100 mL is recalled. The nationwide recall covers 13,000 containers with lot 24A27G66 and expiring 12/31/2025. The FDA lists discoloration as the hazard. Stop using and contact Baxter or a healthcare provider.
Discoloration
Consumers and healthcare providers should stop using this product immediately. Contact Baxter Healthcare Corporation or your healthcare provider for guidance. Notification method: Letter
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Acetaminophen injections are used in clinical settings for pain management and fever control when oral administration is not possible.
Discoloration indicates potential chemical or integrity issues that could affect safety or efficacy.
This recall is not part of a broader industry pattern.
Health care settings may face workflow disruptions and the need to substitute alternate analgesics.
NDC on label, packaging, and accompanying documentation.
Refunds/replacements follow Baxter's recall process, typically weeks to months depending on caseload.
Document recall notice, lot number, expiration, and correspondence with Baxter.
Product: Acetaminophen Injection 1000 mg/100 mL. Container: Viaflo 100 mL. Route: Rx only. Manufacturer: Baxter Healthcare Corporation, Deerfield, IL 60015. Made in Ireland. NDC: 36000-306-60. Quantity: 13,000 containers. Distribution: U.S. nationwide. Lot: 24A27G66. Expiry: 12/31/2025.
No specific injuries or incidents are described in the provided recall data.
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