Argon Medical Devices recalls sterile Luer Lock Plugs due to potential incomplete seal causing sterility loss. Affected units include specific lot numbers from 2022. Consumers should contact the company for details.
The seal formed on the edge of the pouch may be incomplete, which could result in a loss of sterility to the product.
Argon Medical Devices is recalling sterile Luer Lock Plugs that may have an incomplete seal, risking loss of sterility. This could lead to infections if used in medical procedures. The recall affects specific lot numbers sold in 2022.
The seal on the pouch edge might not form properly, which could allow contamination. This loss of sterility might lead to infections during medical procedures if the plugs are used without proper sterility.
Healthcare professionals and medical facilities using the sterile plugs for procedures. Those with the specific lot numbers from the recall list are most at risk.
Check the label for the manufacturer name 'Argon Medical Devices, Inc.' and lot numbers 11228890, 11230669, or 11231874. The product is a sterile Luer Lock Plug sold in boxes of 50.
Reach out to Argon Medical Devices, Inc. for specific instructions on handling affected units.
Argon Medical Devices is recalling sterile Luer Lock Plugs that may have an incomplete seal, risking loss of sterility.
Lot numbers 11228890, 11230669, and 11231874.
Look for the manufacturer name 'Argon Medical Devices, Inc.' and the specific lot numbers listed.
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-0292-2020 — Argon Medical Devices Argon Medical Devices Hello, I own a Argon Medical Devices that is covered by recall Z-0292-2020 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.