Baxter Infusion Pump Injury and Wrongful Death Lawsuit Lawyers

Nationwide Safety Concerns Over Baxter’s Novum IQ Large Volume Pump and Potential Legal Claims for Victims

The U.S. Food and Drug Administration (FDA) has issued an early alert regarding the Baxter Novum IQ Large Volume Pump (LVP) following reports of serious injuries and patient deaths linked to device malfunctions. The infusion pump, widely used in hospitals across the country, is intended to deliver intravenous fluids, medications, and blood products under physician supervision. However, the device has shown a potentially dangerous defect that can cause underinfusion, overinfusion, or total non-delivery of critical medications, posing life-threatening risks to patients.

Baxter has acknowledged receiving at least 79 reports of serious injuries and two deaths associated with this defect. These alarming statistics have prompted a nationwide call for urgent action to protect patient safety.

Details of the Recall and Affected Devices

The affected product, Baxter’s Novum IQ Large Volume Pump, has been flagged for problems during infusion rate changes, particularly when transitioning to a flow rate that is more than double the previous rate. The malfunction may result in partial or complete failure to deliver prescribed treatments, leading to hemodynamic instability, cardiac arrhythmias, insufficient sedation, hyperglycemia, or thromboembolic events.

Additionally, Baxter identified increased reports of incorrect loading of the administration set, which can cause dangerous variations in infusion rates. The recall affects all units under product code 40700BAXUS (UDI-DI 05413765851797) currently in use nationwide.

Hospitals have been instructed to change administration sets or replace affected pumps as soon as it is safe to do so. When immediate replacement isn’t possible, specific steps must be followed to reduce risk, but these measures do not eliminate the underlying defect.

Potential Injuries Linked to the Baxter Infusion Pump Defect

Patients rely on infusion pumps for precise, life-saving drug delivery during hospitalization. A malfunction can have devastating consequences, especially for critically ill patients or those undergoing complex treatments. Known risks include:

• Severe fluctuations in medication dosing
• Prolonged underinfusion or total failure of drug delivery
• Overinfusion leading to toxicity or fluid overload
• Heart rhythm disturbances and blood clots
• Delayed treatment of critical conditions
• In the worst cases, fatal outcomes

Families affected by pump malfunctions may experience unexpected medical complications, additional hospitalization, long-term health consequences, or the loss of a loved one.

Legal Options for Victims of the Baxter Pump Recall

Medical device manufacturers are legally obligated to ensure the safety of their products before they are introduced into patient care. If a defective device causes harm, patients and their families may have grounds to pursue legal claims against Baxter for:

• Medical expenses and additional treatment costs
• Pain, suffering, and emotional distress
• Lost wages or diminished earning capacity
• Wrongful death damages in fatal cases

Holding manufacturers accountable not only provides justice for victims but also helps improve patient safety standards nationwide.

What to Do If You or a Loved One Was Affected

If you or someone close to you suffered complications linked to a Baxter Novum IQ infusion pump, take these steps immediately:

• Request your medical records and confirm whether the recalled device was used.
• Seek a thorough medical evaluation if you experience unexplained health complications following treatment.
• Contact a qualified personal injury attorney to understand your legal rights and potential compensation options.

Prompt legal action can preserve evidence and strengthen your case against negligent medical device manufacturers.

Contact Parker Waichman LLP For A Free Case Review

If you or a loved one experienced complications due to a defective Baxter Novum IQ infusion pump, you may be entitled to financial compensation. Parker Waichman LLP is a national personal injury law firm with extensive experience in defective medical device claims.

Call 1-800-YOUR-LAWYER (1-800-968-7529) now for a free consultation to protect your rights and seek justice for the harm you’ve suffered. Regardless of your location or where your injury occurred, our nationwide product injury law firmis ready to assist you and provide a free consultation.