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device recall
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Baxter Healthcare Corporation device recall (Cls II)

January 13, 2026updated 5mo ago
community read0 votes

Brand Name: Spectrum IQ Product Name: Infusion Pump Model/Catalog Number: 3570009 Software Version: N/A Product Description: Infusion Pump, one unit per carton Component: N/A — Reason: Pumps were released without full testing being performed, including occlusion alarm testing. — Status: Ongoing

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fda device recalls
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same company · ±60 days · 6

  • device 510kBaxter Healthcare Corp/ Excel Medical — WAVE Clinical Platform (2.0.000) (510k cleared)Jan 16, 2026
  • approvalMAGNESIUM SULFATE: MAGNESIUM SULFATE — FDA approvalJan 8, 2026
  • recallBaxter Healthcare Corporation recall (Cls II)Feb 4, 2026
  • approvalNOREPINEPHRINE BITARTRATE: NOREPINEPHRINE BITARTRATE IN 0.9% SODIUM CHLORIDE (NOREPINEPHRINE BITARTRATE) — FDA approvalFeb 6, 2026
  • device 510kBaxter Healthcare Corporation — Welch Allyn FlexiPort Blood Pressure Cuffs (FlexiPort Blood Pressure Cuffs) (510k cleared)Dec 16, 2025
  • device recallBaxter Healthcare Corporation device recall (Cls I)Feb 18, 2026

🐶 often sniffed alongside

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  • 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

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