FDA MedWatch Safety AlertsOriginal article
Epidural Kit Correction: Medical Action Industries Issues Correction for Epidural Kits Containing Spectra Medical Devices Lidocaine Ampules
RegulatoryLidocaine AmpulesSodium Chloride AmpulesNegative
AI Analysis
Summary
Medical Action Industries issued a correction for epidural kits containing recalled sodium chloride ampules from Huons Co. and Spectra Medical Devices lidocaine ampules.
Outcome Details
Product correction issued for epidural kits containing recalled sodium chloride ampules
Importance:3/10
Sentiment:
-0.60
recallproduct_correctionepidural_kitmedical_deviceregulatory
Related Companies
Read the original article
Published by FDA MedWatch Safety Alerts on September 10, 2026 4:00 AM