Fresenius Kabi Recalls Ivenix Pump Over Critical Mechanical Issue
Fresenius Kabi has issued an urgent recall of its Ivenix Large Volume Pump (LVP) for mechanical issues with the fluid valve pins.
Fresenius Kabi has issued an urgent recall of its Ivenix Large Volume Pump (LVP) for mechanical issues with the fluid valve pins.
The BD Alaris Infusion System has received U.S. FDA 510(k) clearance, enabling remediation and a return to full commercial operations.
Fresenius Kabi’s Ivenix Infusion System received an Innovative Technology contract from healthcare performance improvement company Vizient.
Fresenius Kabi has issued an urgent recall of its Ivenix Large Volume Pump (LVP) for mechanical issues with the fluid valve pins.
Smiths Medical has issued an Urgent Medical Device Correction Letter for two potential issues with CADD infusion system infusion sets.
Read MoreB. Braun’s wireless devices of the Space Infusion Pump System has earned certification to UL 2900-2-1 via the UL Cybersecurity Assurance Program.
Read MoreBelow, Ben Noonan, general manager for North America at Eitan Medical, sits down with 24×7 Magazine to shed light on COVID-19’s impact on the infusion therapy device market and share what’s trending from an equipment design perspective.
Read MoreInfusion Associates, provider of medically prescribed outpatient infusion and injection therapies, opened its first Ohio clinic location.
Read MoreCertain Baxter infusion pumps have been discovered to have multiple cybersecurity vulnerabilities, which the company plans to address.
Read MoreThe U.S. FDA has granted 510(k) clearance to Baxter’s Novum IQ syringe infusion pump with Dose IQ Safety Software.
Read MoreHealthIV, a healthcare company focused on improving home health outcomes, is bringing its in-home infusion therapy services to LA.