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device recall
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Baxter Healthcare Corporation device recall (Cls I)

February 18, 2026updated 5mo ago
community read0 votes

Blue Ventilator Adapter Module, single-patient use circuit, Product Code M07937. Accessory to Baxter Volara Respiratory Therapy system. — Reason: Urgent Medical Device Correction for the Volara system single-patient use circuit due to the potential that patients or caregivers may be unaware of a possible decrease in oxygen levels (oxygen desaturation), or potential lung tissue injury from overexpansion (barotrauma) when the Volara device is used in the home care environment. This correction is providing the home caregiver specific instructions for use. — Status: Ongoing

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same company · ±60 days · 6

  • device recallBaxter Healthcare Corporation device recall (Cls II)Feb 18, 2026
  • approvalPHYTONADIONE: PHYTONADIONE — FDA approvalFeb 26, 2026
  • approvalNOREPINEPHRINE BITARTRATE: NOREPINEPHRINE BITARTRATE IN 0.9% SODIUM CHLORIDE (NOREPINEPHRINE BITARTRATE) — FDA approvalFeb 6, 2026
  • recallBaxter Healthcare Corporation recall (Cls II)Feb 4, 2026
  • approvalDoxil: DOXIL (LIPOSOMAL) (DOXORUBICIN HYDROCHLORIDE) — FDA approvalMar 10, 2026
  • device 510kBaxter Healthcare Corp/ Excel Medical — WAVE Clinical Platform (2.0.000) (510k cleared)Jan 16, 2026

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