Home
Drug Information
Sponsors
Ask Duke Using AI
Sign up for Clinical Trials
Coupons
Donation
Others
Forum
CDC Media
FDA Media
FAQs
Login
Register
Home
FDA Media
Alert Detail
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
Recent FDA Updates
FDA Safety Alert
Sodium Chloride Flush Recall: Spectra Medical Removes Sodium...
Sep 18, 2026
FDA Safety Alert
Nitric Oxide Delivery System Correction: NOxBOX Updates Use...
Sep 18, 2026
Drug Shortage
FDA Drug Shortage: Rivastigmine Film, Extended Release
Sep 18, 2026
Back to FDA Media Center
