B. Braun Medical, Inc. is recalling the Infusomat Space Volumetric Infusion Pump System due to faulty occlusion alarms that may lead to interruptions in the delivery of high-risk medications, potentially causing serious harm or death, with 51 complaints, one injury, and one death reported.
These infusion system replacement batteries were recalled because a defect has diminished how long they can be used to run the system, which may cause the system to shut down an ongoing infusion.
IRadimed Corp. issued an Urgent Medical Device Correction Letter regarding a potential issue with some 1057 Syringe Adapter Sets.
B. Braun Medical, Inc. is recalling the Infusomat Space Volumetric Infusion Pump System due to faulty occlusion alarms that may lead to interruptions in the delivery of high-risk medications, potentially causing serious harm or death, with 51 complaints, one injury, and one death reported.
Infusion Associates, provider of medically prescribed outpatient infusion and injection therapies, opened its first Ohio clinic location.
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Certain Baxter infusion pumps have been discovered to have multiple cybersecurity vulnerabilities, which the company plans to address.
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The U.S. FDA has granted 510(k) clearance to Baxter’s Novum IQ syringe infusion pump with Dose IQ Safety Software.
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HealthIV, a healthcare company focused on improving home health outcomes, is bringing its in-home infusion therapy services to LA.
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The FDA issued warning letters to Zyno Medical & InfuTronix for failing to investigate potential product failures linked to company devices.
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Infusion Associates (IA) announced the promotion of its senior VP of revenue cycle to senior VP of corporate development & strategy.
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Smiths Medical is recalling infusion pumps for eight software malfunctions that affect different serial numbers and software versions.
