Medical Action Industries issues correction for epidural kits containing recalled Huons Co. lidocaine ampules

Medical Action Industries has released a correction notice for several of its epidural kit products after discovering that they contain lidocaine ampules from Huons Co. that were previously recalled.

The correction does not require removal of the kits from the market; instead, users are instructed to correct the kits by removing the affected components before further use.

The FDA has classified this recall as the most serious type, indicating that continued use without correction could cause serious injury or death.

A list of the specific kit models and lot numbers affected is provided in the notice, and customers have been advised to follow the correction instructions.