Ivenix Infusion System (IIS), Large Volume Pump LVP-0004
FDA device recall Z-0549-2024 · posted 2023-12-20 · Open, Classified
Recall details
- Recalling firm
- Fresenius Kabi USA, LLC
- Reason for recall
- The device may experience mechanical interference on the Fluid Valve pins, which will trigger a Pump Problem alarm. The issue may lead to delay or interruption of therapy. Depending on the therapy and duration of delay/interruption, the issue may lead to serious harm or death.
- Action taken
- On November 29, 2023, the firm began notifying affected customers via" URGENT-Medical Device Recall" letter dated November 28, 2023. Customers were provided with precautions to take until the affected LVPs are able to be returned for repair or replacement of internal hardware. Customers will be contacted by a Fresenius Kabi service representative to create a plan for addressing any affected LVPs at their facility. This effort is expected to begin in January 2024. Fresenius Kabi will repair LVPs that may encounter mechanical interference causing the Fluid Valve Actuation System not to move properly. If the LVP cannot be repaired, it will be replaced at no cost to the customer. If you have any questions contact Customer support at, email: Ivenix_support@fresenius-kabi.com or phone at 1-978-775-8100.
- Root cause
- Process change control
- Status
- Open, Classified
- Product code
- FRN
- Quantity affected
- 938 US
- Distribution
- US distribution to states of: CA, CO, NJ, UT, and WI.
- Date initiated
- 2023-11-29
- Date posted
- 2023-12-20
- Location
- North Andover, MA
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Related 510(k) clearances
| Record | Firm | Date |
|---|---|---|
| Ivenix Infusion System (IIS) (K183311) | Ivenix, Inc. | 2019-06-07 |