Argon Medical Devices recalls specific Transvenous Pacing Electrode Tray models due to potential sterility issues in lidocaine injection kits. Affected units may not meet safety standards for medical use.
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 Transvenous Pacing Electrode Trays with specific reference numbers because the lidocaine injection kits they contain may not meet sterility standards. This could pose a risk to patient safety during medical procedures.
The recall states that the lidocaine injection kits in these trays may not meet sterility release criteria. This means the kits could be contaminated, potentially causing infections or other complications during medical procedures.
Medical professionals using the recalled electrode trays and patients undergoing procedures with these devices are at risk. The most vulnerable are those receiving treatments involving the lidocaine injection kits.
Check for reference numbers 008416A or 008566A on the electrode tray. The expiration dates listed are July 19, 2027, and December 31, 2026, for the specific lots.
Identify the reference number on the electrode tray to confirm if it matches 008416A or 008566A.
The lidocaine injection kits in these electrode trays may not meet sterility release criteria, which could pose a risk during medical procedures.
The recall record does not specify a remedy, so contact Argon Medical Devices directly for guidance.
Yes, the expiration dates listed are July 19, 2027, and December 31, 2026, for the specific lots.
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-2704-2026 — Argon Medical Devices Argon Medical Devices Hello, I own a Argon Medical Devices that is covered by recall Z-2704-2026 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.
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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.
