Argon Medical Devices recalls specific One-Piece Introducer Trays (REF: 497455, 497434) due to potential sterility issues in lidocaine kits. Affected units have unique serial numbers and expiration dates.
Kits containing Lidocaine HCL Injection USP 1% 10mg/mL 5mL ampules subject to another recall recalled due to not meeting release criteria for sterility.
Argon Medical Devices is recalling certain One-Piece Introducer Trays because the lidocaine injection kits they contain may not meet sterility standards. This could lead to infections if used in medical procedures.
The lidocaine injection kits in these trays may not meet sterility requirements. This could allow bacteria to enter the bloodstream during medical procedures, potentially causing infections.
Healthcare professionals using these trays for cardiovascular procedures are most at risk. Patients receiving procedures with these trays could face infection risks.
Check for product reference numbers 497455 or 497434 on the tray. Look for expiration dates of July 19, 2027, on the packaging.
Verify the reference number and expiration date on the tray packaging to confirm if it is affected.
The lidocaine injection kits in these trays may not meet sterility standards, which could lead to infections during medical procedures.
Check for reference numbers 497455 or 497434 with an expiration date of July 19, 2027.
The recall does not specify a remedy, so contact Argon Medical Devices for further instructions.
We’ve drafted a message you can send Argon Medical Devices to request your refund or repair — edit it as you like.
Subject: Recall Z-2705-2026 — Argon Medical Devices Argon Medical Devices Hello, I own a Argon Medical Devices that is covered by recall Z-2705-2026 from Argon Medical Devices. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
