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Alaris infusion pumps come with a PCU, or point of care unit, and can be customized with up to four modules. These modules are connected to tubes and bags of medicine or other fluids. The modules work together with the PCU to perform a variety of functions.

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Hospitals and health care facilities across the country use these pumps to deliver nutrients, blood products and medications such as insulin, antibiotics, chemotherapy and pain relievers. Trained users, such as nurses, program these pumps to deliver set quantities of medications and fluids into a patient at specific times.

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Modules can be attached to either side of the PCU. These modules perform a variety of tasks from dispensing medication to stopping medication at specific times.

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The Alaris EtCO2 Module helps reduce the risk of opioid-induced respiratory depression. It monitors a patient’s respiratory status and stops medicine infusion if the respiratory status falls. Providers can use this module with the PCU or on its own.

Several recalls of BD Alaris pumps sold in the United States have occurred over the years. The most recent recalls occurred in 2019 and 2020. The recalled models include PCUs, modules and accessories from the 8000 series.

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On Aug. 4, 2020, BD issued a recall for 141,889 of its syringe modules and size sensor kits because PCU units may display the wrong syringe type or size. This could lead to over or under infusion.

BD Alaris Systems infusion pumps monitor a patient’s vital signs and deliver medications, blood and fluids into a patient’s body in controlled amounts. Health care facilities and hospitals use these pumps in adults and children.

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This module helps ensure accurate medication delivery. It works with various syringe sizes and provides a wide range of flow rates.

Health care professionals use the BD Alaris pump module for large volume infusions in pediatric, neonatal or adult patients. Up to four of these modules can attach to the PCU and dispense four different infusions.

The Syringe Module delivers medications, fluids, blood products and blood. The flow of medication is continuous or intermittent.

The company recalled the devices because one or more keys on the keypad could become stuck or unresponsive. This could prevent clinicians from changing medication or fluid infusions and infusion delay.

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Becton, Dickinson and Company (BD) manufactures the BD Alaris Systems pumps. The U.S. Food and Drug Administration allowed the first models onto the market in the 1990s. The agency has since cleared more models for sale.

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BD determined that the thickness of silicone segments of the tubing was not uniform. This could cause the tubing to fail or become blocked. The recall was associated with reports of injuries, some of which were serious.

BD has issued several recalls for these pumps and pump modules because of software and hardware problems that can cause serious injuries and death.

Our team includes experienced medical writers, award-winning journalists, researchers and certified medical and legal experts. Drugwatch.com is HONCode (Health On the Net Foundation) certified. This means the high-quality information we provide comes from credible sources, such as peer-reviewed medical journals and expert interviews.

On Feb. 4, 2020, BD recalled 774,000 various Alaris series 8000 PCUs and modules. Some of these recalled pumps were distributed as far back as July 2004.

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The BD Alaris PC Unit or Point of Care Unit (PCU) is the “brain” of the pump system. It has a display and keypad on it. It’s what a trained care professional uses to program the pump with a specific amount of medicine to deliver into a patient, when to deliver it and other specific instructions. Some hospitals or facilities have pre programmed these settings into the PCU.

On May 6, 2019, BD recalled 151,139,816 Alaris Pump Model 8100 infusion sets manufactured between May 2016 and March 2019. The pumps could deliver medications too quickly or deliver medications while the pump was not in “running status.”

The Auto-ID Module allows providers to scan barcodes that provide information such as the patient ID, clinician ID and drug information. This information goes into the PCU.

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The FDA classified this as a class one recall — the agency’s most severe. This means the devices can cause serious injuries or death.

Drugwatch.com has provided reliable, trusted information about medications, medical devices and general health since 2008. We’ve also connected thousands of people injured by drugs and medical devices with top-ranked national law firms to take action against negligent corporations. Our team includes experienced medical writers, award-winning journalists, researchers and certified medical and legal experts. Drugwatch.com is HONCode (Health On the Net Foundation) certified. This means the high-quality information we provide comes from credible sources, such as peer-reviewed medical journals and expert interviews. The information on Drugwatch.com has been medically and legally reviewed by more than 30 expert contributors, including doctors, pharmacists, lawyers, patient advocates and other health care professionals. Our writers are members of professional associations, including American Medical Writers Association, American Bar Association, The Alliance of Professional Health Advocates and International Society for Medical Publication Professionals. About Drugwatch.com Assisting patients and their families since 2008. Helped more than 12,000 people find legal help. A+ rating from the Better Business Bureau. 5-star reviewed medical and legal information site. Learn More About Us Testimonials "Drugwatch opened my eyes to the realities of big pharmacy. Having a family member with major depression and anxiety, I was looking for information on her medications. I found information that was very helpful, that her psychiatrist never told her." Marianne Zahren Patient’s Family Member

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Drugwatch.com has provided reliable, trusted information about medications, medical devices and general health since 2008. We’ve also connected thousands of people injured by drugs and medical devices with top-ranked national law firms to take action against negligent corporations. Our team includes experienced medical writers, award-winning journalists, researchers and certified medical and legal experts. Drugwatch.com is HONCode (Health On the Net Foundation) certified. This means the high-quality information we provide comes from credible sources, such as peer-reviewed medical journals and expert interviews. The information on Drugwatch.com has been medically and legally reviewed by more than 30 expert contributors, including doctors, pharmacists, lawyers, patient advocates and other health care professionals. Our writers are members of professional associations, including American Medical Writers Association, American Bar Association, The Alliance of Professional Health Advocates and International Society for Medical Publication Professionals. About Drugwatch.com Assisting patients and their families since 2008. Helped more than 12,000 people find legal help. A+ rating from the Better Business Bureau. 5-star reviewed medical and legal information site. Learn More About Us Testimonials "Drugwatch opened my eyes to the realities of big pharmacy. Having a family member with major depression and anxiety, I was looking for information on her medications. I found information that was very helpful, that her psychiatrist never told her." Marianne Zahren Patient’s Family Member

On Aug. 4, 2020, BD recalled 305,526 BD Alaris PC Unit 8015 models and keypad replacement kits manufactured from April 7, 2017 to June 15, 2020.

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BD said system errors could lead to over or under infusion and interruption of infusion. At the time of the recall, BD was aware of 55 reported injuries and one death.

At the time of the announcement, BD was aware of 1,186 complaints and one reported injury. At the time, there were no reported deaths.

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A 2022 report noted that up to 75% of IV pumps have vulnerabilities that could threaten patient safety if exploited. Because these defects may cause serious injuries or death, lawyers are filing BD Alaris Systems lawsuits on behalf of patients injured after using these pumps.

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