device recall
saveBaxter Healthcare Corporation device recall (Cls I)
August 4, 2025updated 6mo ago
community read0 votes
Novum IQ Syringe Pump, Product Code 40700BAX, infusion pump — Reason: 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). — Status: Ongoing
view source ↗Data sources
last refreshed 6mo ago
Found something off?
same company · ±60 days · 6
- device recallBaxter Healthcare Corporation device recall (Cls I)Aug 4, 2025
- device recallBaxter Healthcare Corporation device recall (Cls I)Aug 4, 2025
- device recallBaxter Healthcare Corporation device recall (Cls II)Aug 8, 2025
- device 510kBaxter Healthcare Corporation — Spectrum IQ Infusion System with Dose IQ Safety Software (3570009) (510k cleared)Jul 28, 2025
- device 510kBaxter Healthcare Corporation — SIGMA Spectrum Infusion Pump with Master Drug Library (510k cleared)Jul 28, 2025
- device 510kBeckman Coulter, Inc. — MicroScan Dried Gram-Positive MIC/Combo Panels with Daptomycin (DAP) (0.06-32 µg/mL) (510k cleared)Aug 15, 2025
🐶 often sniffed alongside
top 8- tagRecall41 co-mentions · 32 sources
- tagDrug Shortage15 co-mentions · 15 sources
- tagAdCom9 co-mentions · 9 sources
- tag510(k) Clearance6 co-mentions · 6 sources
- tagHematology4 co-mentions · 2 sources
- tagPMA Approval3 co-mentions · 3 sources
- tagOphthalmology2 co-mentions · 1 sources
- tagCardiology2 co-mentions · 2 sources
comments(0)
5-min edit window · permanent after that