{"url_path":"/fda/device/recalls/Z-3065-2026","section_key":"summary","section_title":"DEVICE Recall: Baxter Healthcare Corporation — Baxter Novum IQ Syringe Pump, Model Number 40800BAXUS","topic":"fda","document":{"doc_type":"device-recall","doc_date":"2026-08-11","source_url":"https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3065-2026%22","accession_number":null,"cik":null,"ticker":null,"issuer_name":null,"edgar_url":null,"primary_entity_key":null,"primary_entity_name":"Baxter Healthcare Corporation"},"word_count":128,"has_tables":false,"body_markdown":"# FDA DEVICE Recall: Z-3065-2026\n\n**Recalling firm:** Baxter Healthcare Corporation\n**Classification:** Class II\n**Status:** Ongoing\n**Type:** Voluntary: Firm initiated\n**Initiated:** 2026-08-11\n**Report date:** 2026-09-09\n\n## Product\nBaxter Novum IQ Syringe Pump, Model Number 40800BAXUS\n\n## Reason\nA software issue that may occur during a Volume/Time (VOT) multi-syringe infusion when a syringe reaches empty and is replaced while a Volume To Be Infused (VTBI) remains.\n\n## Affected lots\nUDI-DI 05413765852428, all serial numbers\n\n## Distribution\nUS Nationwide distribution including in the states of AK, AL, AR, AZ, CA, CO, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, SC, SD, TN, TX, UT, VA, VT, WA, WI, and WV."}