banner
Home / News / FDA issues recall on infusion pump parts due to risk of uncontrollable drug flow
News

FDA issues recall on infusion pump parts due to risk of uncontrollable drug flow

Oct 15, 2024Oct 15, 2024

The U.S. Food and Drug Administration (FDA) has issued a recall on behalf of Fresenius Kabi for a specific lot of the company’s Ivenix infusion pumps—specifically the administrative sets on those systems. The recall was voluntarily initiated due to a manufacturing error that could cause medication to flow at an uncontrollable rate.

Ivenix infusion systems work like many other pumps, utilizing air pressure to precisely control the flow of liquids—typically containing drugs—as they are administered to patients. These particular devices are primarily used in hospitals and outpatient clinics, where use of systems must cease immediately.

Due to the serious risk of potentially fatal overdose, the FDA has labeled this recall the most serious of its kind. There have been two reported injuries, but no deaths have been linked to the malfunctioning administrative sets on the pumps.

The recall is for one specific lot of Ivenix LVP Primary Administration Sets, of which only 25 were manufactured. The details are as follows:

Fresenius Kabi sent a letter Aug. 2 to all impacted customers that should contain instructions on how to replace the recalled administrative set on the pumps. After immediately removing the infusion pumps from care settings and ensuring they cannot be used, customers can return affected units to the company for a replacement.

Anyone with one of the pumps with a defective administrative set should contact Fresenius Kabi Customer Service at 855-354-6387 to initiate a return. Customers must submit a reply form to receive a replacement product.

The FDA and Fresenius Kabi also ask that providers share the recall notice to ensure all potentially dangerous devices are removed from supply. The notice can be found here.

Chad is an award-winning writer and editor with over 15 years of experience working in media. He has a decade-long professional background in healthcare, working as a writer and in public relations.

When drugs are on the FDA’s shortage list, outsourcing facilities can produce their own compounded versions. When the FDA removed tirzepatide from that list with no warning, it created a considerable amount of chaos both behind the scenes and in pharmacies all over the country.

If passed, this bill would help clinician-led clinical registries explore Medicare data for research purposes. The Society of Thoracic Surgeons and American College of Cardiology both shared public support for the bipartisan legislation.

Cardiologists and other physicians may soon need to provide much more information when ordering remote patient monitoring for Medicare patients.

What is being recalled?Product Name: Unique Device Identifier (UDI)Lot Number:Next steps