⚠ RecallRadar📷 ScanGuidesOfficial U.S. recall notices, restated plainly

Fresenius Kabi USA, LLC: Ivenix Infusion System (IIS), Large Volume Pump. Model Number: LVP-0004.

Medical DevicesSource: FDA (device) · Date: 2025-11-05

Read the official notice at FDA (device) →

Share on XFacebookRedditEmail

Get alerts for Fresenius Kabi

Guides: Which agency handles which recall (FDA vs USDA vs CPSC vs NHTSA)

The text below is copied from the official FDA (device) record. If anything differs, the official notice is correct.

Company / brand
Fresenius Kabi USA, LLC
Product
Ivenix Infusion System (IIS), Large Volume Pump. Model Number: LVP-0004.
Reason / hazard
Potential issue that can cause the device to register "phantom" touches in the lower-left corner of the touchscreen during operation.
Classification
Class II
Status
Ongoing
Distribution / sold at
US Nationwide distribution in the state of Minnesota.
Recall initiated
2025-09-03
Code info
Model Number: LVP-0004. UDI-DI: 00811505030320. Serial Numbers: 2318600378, 2321600176, 2333300359, 2403001383, 9242756430, 9243097443.
Product quantity
6 units
Voluntary mandated
Voluntary: Firm initiated
City
North Andover
State
MA
Country
United States
Event id
97554
Free daily digest + "My products" watchlist

Get the daily digest, and tell us what to watch. Everything is optional except your email.

Free allergen alerts:

Categories:

Privacy: we store only what you enter here, use it only to send recall alerts you asked for, never sell or share it, and you can unsubscribe anytime. Double opt-in: we will email you a confirmation link before sending anything; alerts start only after you confirm. Every email has unsubscribe and manage-watchlist links.