FDA Media Alert Detail

FDA Safety Alert

Epidural Kit Correction: Medical Action Industries Issues Correction for Epidural Kits Containing Spectra Medical Devices Lidocaine Ampules

  • U.S. Food and Drug Administration
  • September 10, 2026
  • ID: http://www.fda.gov/medical-devices/medical-device-recalls-and-early-alerts/epidural-kit-correction-medical-action-industries-issues-correction-epidural-kits-containing-spectra

FDA MedWatch Safety Alert

Medical Action Industries is correcting epidural kits containing recalled Huons Co. sodium chloride ampules.
Content syndicated from the official FDA MedWatch Safety Alerts and Adverse Event Reporting Program.
View Official Announcement on FDA.gov

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