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News(10)

• FDA issues alert in wake of BD recall of faulty needle sets
  The FDA’s Center for Devices and Radiological Health issued an early alert for Becton Dickinson’s Intraosseous Vascular Access system needle sets in the wake of four deaths and 45 serious injuries…
  fiercebiotech · 4d ago
• Fresenius Kabi Issues Nationwide Recall of Tyenne® (tocilizumab-aazg) Injection 400 mg/20 mL Vials Due to Presence of Glass Particles
  FOR IMMEDIATE RELEASE – August 10, 2026 – LAKE ZURICH, Ill.— Fresenius Kabi, an operating company of the Fresenius Group, is recalling one lot of Tyenne® (tocilizumab-aazg) Injection 400 mg/20 mL (…
  fda_recalls · 4d ago
• Fresenius Kabi Issues Voluntary Nationwide Recall of One Lot of Morphine Sulfate Injection, USP in a Simplist® Prefilled Syringe Due to Labeling Mix-up
  FOR IMMEDIATE RELEASE – 8/4/2026 – LAKE ZURICH, Ill.— Fresenius Kabi, an operating company of the Fresenius Group, is voluntarily recalling one lot of Morphine Sulfate Injection USP, Simplist® 2 mg…
  fda_recalls · 10d ago
• Convenience Kit Correction: Medical Action Industries Issues Correction for Kits Containing Recalled Namic Manifolds
  Particulates have the potential to be introduced into blood circulation and become lodged within blood vessels.
  fda_medwatch · 11d ago
• Convenience Kit Correction: Argon Medical Issues Correction for Convenience Kits Containing Spectra Medical Device Lidocaine Ampules
  Argon Medical is correcting affected convenience kits by removing included Spectra Medical Devices Lidocaine Ampules.
  fda_medwatch · 15d ago
• Opinion: The growing fang-to-pharmacy pipeline
  “Some of the most powerful medicines we will ever find are already here, carried in the fangs, stingers, and saliva of creatures we’ve been taught to fear,” writes Steve Midway.
  stat · 29d ago
• Convenience Kit Correction: Arrow International Issues Correction for Convenience Kits Containing Recalled Huons Lidocaine and Bupivacaine and Saline
  Saline, Lidocaine and Bupivacaine from affected convenience kits should not be used.
  fda_medwatch · 29d ago
• Early Alert: Convenience Kit Issue from Medical Action Industries
  Particulates have the potential to be introduced into blood circulation and become lodged within blood vessels.
  fda_medwatch · 1mo ago
• Infusion Pump Correction: Fresenius Kabi Issues Correction for dropped or jarred Ivenix Large Volume Infusion Pumps
  If dropped, the Ivenix pump touchscreen may become unresponsive and should be removed from use.
  fda_medwatch · 1mo ago
• Infusion Pump Correction: Fresenius Kabi Issues Correction for Ivenix Large Volume Infusion Pump
  A software anomaly may cause a false battery-health value. The pump should remain plugged in at all times.
  fda_medwatch · 1mo ago