FDA MedWatch Safety AlertsUnited States10 September 2026
Epidural Kit Correction: Medical Action Industries Issues Correction for Epidural Kits Containing Spectra Medical Devices Lidocaine Ampules
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Firsthand records what FDA MedWatch Safety Alerts announced and links to the original. The wording below is theirs, not ours.
Medical Action Industries is correcting epidural kits containing recalled Huons Co. sodium chloride ampules.
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