Safety Alert: Class I: Baxter Healthcare Corporation is issuing an Urgent Medical Device Correction for the Novum IQ Large Volume Pump (LVP) and Novum IQ Syringe Pump (SP) due to software anomalies that may result in a blank Run screen (LVP and SP) and/or false motor movement system error (SP only).
healthClass IRecalled on Sep 10, 2025
Novum IQ Syringe Pump, Product Code 40700BAX, infusion pump
🔢 22703 units
Sold At: Baxter Healthcare Corporation(US distribution including Puerto Rico and OUS (International) Canada)
Recall #: FDA-DEVICE-Z-2334-2025
Source: FDA-ENFORCEMENT
Product Identification
- Lot/Batch Codes:
- UDI/DI N/A, All Serial Numbers
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Summary
Baxter Healthcare Corporation is issuing an Urgent Medical Device Correction for the Novum IQ Large Volume Pump (LVP) and Novum IQ Syringe Pump (SP) due to software anomalies that may result in a blank Run screen (LVP and SP) and/or false motor movement system error (SP only).
What to do next
- 1URGENT: Stop using this product immediately - serious health hazard
- 2Check with retailer or manufacturer for recall status and remedy options
- 3Contact Baxter Healthcare Corporation for return or refund information
- 4Visit the official FDA recall page for complete details
Summaries only; always follow the official notice.