FDA: Convenience Kit Correction: Argon Medical Issues Correction for Convenience Kits Containing Spectra Medical Device Lidocaine Ampules
Published: 07/30/2026
Sources:
- Food and Drug Administration
Relevant To:
- Ambulatory Surgical Centers,
- Rural Emergency Hospitals,
- Critical Access Hospitals,
- Hospitals,
- Office-Based Surgery
The Food and Drug Administration (FDA) is aware that Argon Medical has issued a letter to affected customers recommending certain convenience kits be corrected prior to continued use by removing components affected by the Huons Co., Ltd. recall.
The recall includes specific Argon Medical kits containing Spectra Medical Device, Inc. pain management kits with Huons lidocaine HCL Injection.
- Huons Co., Ltd. initiated a recall of Bupivacaine HCL in Dextrose Injection