Argon Medical Devices recalls T-Lok Bone Marrow Trays with specific serial numbers due to potential sterility issues. 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 specific T-Lok Bone Marrow Trays because the lidocaine injection kits inside them were found not to meet sterility standards. This could lead to infections if used in medical procedures.
The lidocaine injection kits in the recalled trays were found not to meet sterility requirements. This means the kits could be contaminated, potentially causing infections during medical procedures.
Healthcare professionals using the T-Lok Bone Marrow Trays with the listed serial numbers are affected. Patients receiving procedures using these trays may be at risk of infection.
Check the product reference numbers: BMT1104STL, BMET1104TL, or BMT1104CATL. The expiration dates on the packaging are 11/30/2026 or 3/31/2028.
Verify the reference number on the tray packaging to confirm if it matches BMT1104STL, BMET1104TL, or BMT1104CATL.
The lidocaine injection kits in the recalled trays were found not to meet sterility standards, which could lead to infections during medical procedures.
Check the reference number on the packaging. If it matches BMT1104STL, BMET1104TL, or BMT1104CATL, contact Argon Medical Devices for further instructions.
The recall is due to potential contamination from the lidocaine kits, which could cause infections. Serious injury is not mentioned in the recall notice.
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-2707-2026 — Argon Medical Devices Argon Medical Devices Hello, I own a Argon Medical Devices that is covered by recall Z-2707-2026 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.
