Quick Facts at a Glance
- Recall Date
- January 13, 2026
- Hazard Level
- HIGH
- Brand
- Baxter Healthcare
- Category
- Health & Personal Care
- Sold At
- Multiple Retailers
- Geographic Scope
- 1 states
- At-Risk Groups
- GENERAL
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 - Medical Devices; 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
- Product type
- Infusion Pump
- Model numbers
- Lot Code: GTIN 00085412610900, Serial Numbers 3815663, 3823468, 3824743, 3825234, and 3825599
- Sold at
- Multiple Retailers
- Where affected
- OH
Recall Timeline
Key dates and source checks for this recall record.
Recall announced
January 13, 2026
Reported by FDA DEVICE
February 25, 2026
RecallRadar source check
March 4, 2026
Consumer action
Use the official remedy and keep documentation.
Hazard Information
Pumps were released without full testing being performed, including occlusion alarm testing.
What You Should Do
Patients and healthcare providers should stop using this device immediately. Follow the recall instructions provided by the manufacturer. Contact Baxter Healthcare Corporation or your healthcare provider for instructions. Notification method: Telephone
About This Product
An infusion pump is a medical device used to deliver fluids, medication, or nutrients to patients in a controlled manner. Healthcare providers rely on these devices for accurate and timely infusion, making their reliability essential for patient safety.
Why This Is Dangerous
The infusion pumps in question were released without adequate testing, particularly lacking checks on occlusion alarms that alert users to blockages in the infusion line. This defect could lead to dangerous situations where patients do not receive necessary medication.
Industry Context
This recall is not part of a broader industry pattern.
Real-World Impact
The recall affects a small number of units but poses a significant risk due to the potential for improper medication delivery. Patients and healthcare providers must take immediate action to prevent any adverse events.
Practical Guidance
How to identify if yours is affected
- Verify the model number as 3570009.
- If any of these match, your product is affected.
Where to find product info
Serial numbers are typically located on the device label or packaging.
What timeline to expect
Expect a processing time of 4-6 weeks for refunds or replacements.
If the manufacturer is unresponsive
- Document all communications with Baxter Healthcare.
- Reach out again via phone or email for follow-up.
How to prevent similar issues
- Look for FDA approval and testing certifications when purchasing medical devices.
- Consider purchasing devices from reputable manufacturers with a strong track record of safety compliance.
Documentation advice
Keep records of your purchase, including receipts and any correspondence regarding the recall.
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Product Details
The recall involves Baxter Healthcare's infusion pump, model number 3570009. The product was distributed in Ohio, United States. Five units were recalled.
Key Facts
- Recalled on January 13, 2026
- Five units involved
- Distributed in Ohio, United States
- Immediate stop-use recommendation
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Safety Guide
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