Argon Medical Devices recalls bone marrow trays with specific serial numbers due to potential sterility issues in lidocaine injections. 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 bone marrow trays with certain serial numbers because the lidocaine injections included in them may not meet sterility standards. This could pose a risk of infection during medical procedures.
The lidocaine injections in the recalled trays may not meet sterility standards, which could lead to infections if used in medical procedures. This issue arises from the product not meeting release criteria for sterility.
Medical professionals using bone marrow trays with the specified serial numbers are affected. Patients undergoing procedures with these trays may be at risk of infection.
Check the serial number on the bone marrow tray, which includes codes like CB0033TL or CB0355TLA. The expiration date on the packaging is listed as 3/31/2028 for some units.
Look for serial numbers such as CB0033TL or CB0355TLA on the bone marrow tray packaging.
The lidocaine injections in the recalled bone marrow trays may not meet sterility standards, which could lead to infections during medical procedures.
Check the serial number on the bone marrow tray to see if it matches the recalled numbers. If it does, contact Argon Medical Devices for further instructions.
The recall is due to potential sterility issues, which could lead to infections, but the product does not pose a risk of serious injury in normal use.
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-2709-2026 — Argon Medical Devices Argon Medical Devices Hello, I own a Argon Medical Devices that is covered by recall Z-2709-2026 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.
