FDA recall record

Fresenius Kabi USA Ivenix Infusion System (IIS), Large Volume Pump, Model No recall — FDA Z-1313-2023

Fluid ingress that can cause a loss of electrical funtion and failure of the Set ID Sensory, resulting in the prevention of infusion or halt of infusion.

Class Iclassification
Z-1313-2023official record ID
Apr 19, 2023report date

Recall record at a glance

Official recordZ-1313-2023
CategoryMedical Device Recalls
ClassificationClass I
FDA record statusOngoing
Recalling firmFresenius Kabi USA, LLC
Report dateApr 19, 2023
Recall initiation dateMar 10, 2023
Quantity1,546 units
LocationNorth Andover, MA, United States

Official product description

Ivenix Infusion System (IIS), Large Volume Pump, Model No. LVP-0004

Why the product was recalled

Fluid ingress that can cause a loss of electrical funtion and failure of the Set ID Sensory, resulting in the prevention of infusion or halt of infusion.

Distribution information

Domestic: CA, CO, NJ, WI, & UT. No foreign distribution.

How to read the classification

FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: E-Mail.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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