Baxter Healthcare recalled five infusion pumps on January 13, 2026. The pumps were released without full testing, including critical occlusion alarm checks. Healthcare providers and patients must stop using the device immediately.
Pumps were released without full testing being performed, including occlusion alarm testing.
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
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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.
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.
This recall is not part of a broader industry pattern.
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.
Serial numbers are typically located on the device label or packaging.
Expect a processing time of 4-6 weeks for refunds or replacements.
Keep records of your purchase, including receipts and any correspondence regarding the recall.
The recall involves Baxter Healthcare's infusion pump, model number 3570009. The product was distributed in Ohio, United States. Five units were recalled.
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