Baxter Healthcare Corporation recalled 13,000 containers of Acetaminophen Injection on August 20, 2025. The recall follows reports of discoloration that may affect product safety. Consumers should stop using the medication immediately and contact their healthcare providers for guidance.
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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The recall involves Acetaminophen Injection 1000 mg/100 mL packaged in 100 mL Viaflo containers. The product is available by prescription only and has a lot number of 24A27G66 with an expiration date of December 31, 2025.
The discoloration of the Acetaminophen Injection poses potential safety risks. This defect falls under Class II recall, indicating a moderate risk of adverse health consequences.
As of now, there are no reported injuries or incidents related to the discoloration of this product. Consumers are urged to remain vigilant and report any adverse effects to their healthcare provider.
Stop using the Acetaminophen Injection immediately. Contact Baxter Healthcare Corporation or your healthcare provider for further instructions. Notifications have been sent via letter.
For more information, consumers can reach Baxter Healthcare Corporation at 1-800-XXX-XXXX. Additional details are available at the FDA's recall page.
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