FDA Media Alert Detail

FDA Safety Alert

Sodium Chloride Flush Recall: Spectra Medical Removes Sodium Chloride Injection USP Ampules

  • U.S. Food and Drug Administration
  • September 18, 2026
  • ID: http://www.fda.gov/medical-devices/medical-device-recalls-and-early-alerts/sodium-chloride-flush-recall-spectra-medical-removes-sodium-chloride-injection-usp-ampules

FDA MedWatch Safety Alert

Spectra Medical Devices is removing Sodium Chloride Flush products that were manufactured by Huons Co,. Ltd.
Content syndicated from the official FDA MedWatch Safety Alerts and Adverse Event Reporting Program.
View Official Announcement on FDA.gov

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