Ivenix Infusion System (IIS), Large Volume Pump, Model Number: LVP-0004
FDA device recall Z-0763-2025 · posted 2025-01-08 · Open, Classified
Recall details
- Recalling firm
- Fresenius Kabi USA, LLC
- Reason for recall
- Potential pneumatic valve failure that may cause the LVP to stop an active infusion and/or could prevent the pump from being used.
- Action taken
- Fresenius Kabi notified consignees on 12/06/2024 via "URGENT - Medical Device Recall" letter. Consignees were instructed to do the following: 1. Review the facilities list of affected Serial Numbers and post the list in a public place. 2. If an LVP exhibits a Pump Problem during use, remove the LVP from circulation, and notify Fresenius Kabi. 3. Inform potential users of the product within your organization of this notification. 4. Notify customers if product was further distributed. 5. Complete and return the Customer Reply Form included in the letter to acknowledge receipt. Customers will be contacted by a Fresenius Kabi service representative to create a plan for repairing any affected LVPs at your facility at no cost. Fresenius Kabi will also repair LVPs that may encounter pneumatic valve failures at no additional charge. For customer support and questions, call 1-855-354-6387 normal hours are from Monday thru Friday 8:30am-5pm Easter Time, after hours supported by voicemail messaging or email: Ivenix_support@fresnius-kabi.com.
- Root cause
- Process control
- Status
- Open, Classified
- Product code
- FRN
- Quantity affected
- 1,520 units
- Distribution
- US distribution to states of: ID, MN, NV, TX, VA, WI.
- Date initiated
- 2024-12-06
- Date posted
- 2025-01-08
- 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 |