Quick Facts at a Glance
- Recall Date
- August 20, 2025
- Hazard Level
- HIGH
- Brands
- Baxter Healthcare Corporation, Acetaminophen
- Category
- Health & Personal Care
- Sold At
- Unknown
- Geographic Scope
- 1 states
- At-Risk Groups
- GENERAL, PREGNANT
What to Do Now
Use this page like a recall checklist: verify the product first, then act on the official remedy.
Immediate steps
- 1Stop using the product until you confirm whether it is included in the recall.
- 2Compare the product label, model number, UPC, color, size, and purchase location against the identifiers below.
- 3Follow the official remedy from FDA - Drug Safety; save photos, receipts, labels, and correspondence before contacting the company.
- 4If the product could harm a child, older adult, pet, or patient, move it out of reach immediately.
Check these identifiers
- Brand
- Baxter Healthcare Corporation, Acetaminophen
- Product type
- Acetaminophen Injection
- Model numbers
- Lot #: 24A27G66, Exp 12/31/2025
- UPC codes
- 36000-306, 36000-372, 36000-306-60, 36000-372-40
- Sizes
- 100 mL
- Sold at
- Unknown
- Where affected
- ALL
Recall Timeline
Key dates and source checks for this recall record.
Recall announced
August 20, 2025
Reported by FDA DRUG
September 3, 2025
RecallRadar source check
April 18, 2026
Consumer action
Use the official remedy and keep documentation.
Hazard Information
Discoloration
What You Should Do
Consumers and healthcare providers should stop using this product immediately. Contact Baxter Healthcare Corporation or your healthcare provider for guidance. Notification method: Letter
About This Product
Acetaminophen injections are used in clinical settings for pain management and fever control when oral administration is not possible.
Why This Is Dangerous
Discoloration indicates potential chemical or integrity issues that could affect safety or efficacy.
Industry Context
This recall is not part of a broader industry pattern.
Real-World Impact
Health care settings may face workflow disruptions and the need to substitute alternate analgesics.
Practical Guidance
How to identify if yours is affected
- Verify container is 100 mL Viaflo
- Inspect Lot 24A27G66 and Exp 12/31/2025
Where to find product info
NDC on label, packaging, and accompanying documentation.
What timeline to expect
Refunds/replacements follow Baxter's recall process, typically weeks to months depending on caseload.
If the manufacturer is unresponsive
- Escalate to FDA recall contacts
- File a complaint with the FDA if needed
How to prevent similar issues
- Verify NDC and lot numbers before use
- Keep recall communication and letters for records
- Consult pharmacist before substituting medications
Documentation advice
Document recall notice, lot number, expiration, and correspondence with Baxter.
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Product Details
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.
Reported Incidents
No specific injuries or incidents are described in the provided recall data.
Key Facts
- Lot 24A27G66
- Distribution nationwide in the USA
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Safety Guide
Not sure what to do next? Our guide walks you through the process step by step.
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