Z-2274-2026 Class II Ongoing

Recalled by Fresenius Kabi USA, LLC — North Andover, MA

FDA device recall Z-2274-2026 was initiated by Fresenius Kabi USA, LLC on February 4, 2026 and is designated Class II. Reason for recall: Potential for the Cassette Loading Lever to break. The recall status is ongoing. Affected quantity: 18,444 installed bases.

Recall Details

Product Type
Devices
Report Date
June 10, 2026
Initiation Date
February 4, 2026
Termination Date
N/A
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
18,444 installed bases

Product Description

The Large Volume Pump (LVP) of the Ivenix Infusion System (IIS). Model Number: LVP-0004.

Reason for Recall

Potential for the Cassette Loading Lever to break.

Distribution Pattern

US Nationwide distribution in the states of CA, CO, FL, GA, ID, IL, MA, MD, ME, MI, MN, MS, NE, NJ, NV, OK, OR, SC, TX, VA, WA, WI.

Code Information

Model Number: LVP-0004. UDI-DI: 00811505030320