Z-2274-2026 Class II Ongoing
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