LVP software of the Ivenix Infusion System (IIS); Product Code LVP-SW-0005.
USLVP software of the Ivenix Infusion System (IIS); Product Code LVP-SW-0005.
Recalling Firm: Fresenius Kabi USA, LLC
Motivo del Retiro / Peligro
TranslatedPotential software anomaly that can cause the pump to report a false battery-health value (typically 69%) and trigger a battery-depletion alarm that will shut down the pump unless it is reconnected to AC mains power.
Descripción del Producto e Identificación
TranslatedLVP software of the Ivenix Infusion System (IIS); Product Code LVP-SW-0005.
Additional Source Details
| Field | Value |
|---|---|
| City | North Andover |
| State | MA |
| Event id | 98929 |
| Address 1 | 50 High St Ste 50 |
| Code info | Product Code LVP-SW-0005. UDI-DI: 00811505030122. Software Version 5.10.2 |
| Postal code | 01845-2620 |
| Report date | 20260610 |
| Product type | Devices |
| Product quantity | 32 systems |
| Reason for recall | Potential software anomaly that can cause the pump to report a false battery-health value (typically 69%) and trigger a battery-depletion alarm that will shut down the pump unless it is reconnected to AC mains power. |
| Voluntary mandated | Voluntary: Firm initiated |
| Recall initiation date | 20260506 |
| Initial firm notification | Letter |
| Center classification date | 20260603 |
Consumer Action Protocol: What You Should Do Immediately
Safety StepsInspect the NDC code, batch number, or control number on your medicine bottle or blister packaging to confirm whether your unit is included.
Do not abruptly stop critical prescribed medication without physician advice. Contact your dispensing pharmacist immediately for a safe alternative.
Under statutory consumer protection rules, consumers are entitled to a full refund, certified replacement, or free repair kit without needing the original sales receipt.
If you suffered an injury, illness, or property damage from this product, file an official incident report with regulatory authorities (FDA Devices).
Your Legal Rights as a Consumer
Recalls are legally binding corrective safety actions overseen by statutory government bodies. Recalling entities are legally prohibited from charging consumers for official safety remedies. If a retailer or dealership refuses your recall remedy, notify the issuing regulatory agency immediately.
Frequently Asked Questions About This Recall
FAQ GuideQ1:What should I do immediately if I own or bought LVP software of the Ivenix Infusion System (IIS); Product Code LVP-SW-0005.?
Check the lot number and NDC on your prescription label. For essential medications, consult your doctor or dispensing pharmacist immediately before abruptly stopping your dose.
Q2:Can I get a full refund or free repair for this recall?
Yes. Recalling manufacturers and retail merchants are required under consumer protection regulations to offer a statutory remedy—typically a full refund, certified repair kit, or replacement unit.
Q3:Do I need my original sales receipt to claim a remedy or refund?
In most recall cases, no receipt is required. Because safety recalls are matters of public health and statutory compliance, retailers and manufacturers routinely issue refunds, store credit, or replacement kits upon presentation of the affected product or lot code.
Q4:Where can I verify official information for this safety alert?
This safety alert is aggregated directly from official regulatory agency records (FDA Devices). You can click the 'Official Agency Alert' link on this page to view the primary government notice and contact the manufacturer directly.
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Resumen
- Empresa ResponsableFresenius Kabi USA, LLC
- StatusOngoing
- Nivel de RiesgoClass I
- DistributionUS Nationwide distribution in the states of CA, CO, FL, GA, GA, ID, IL, MD, MI, MN, MO, MS, NE, NJ, NV, OK, OR, SC, TX, VA, WA, WI.
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🚨 SAFETY ALERT: Fresenius Kabi USA, LLC - LVP software of the Ivenix Infusion System (IIS); Product Code LVP-SW-0005. Check if your household is affected: https://therecallfile.com/es/recalls/lvp-software-of-the-ivenix-infusion-system-iis-product-code-lvp-sw-000/FDA-Z-2223-2026
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