Argon Medical Devices recalls specific stopcock models due to potential incomplete seal causing loss of sterility. Affected products include 6 types with lot numbers; users should check their product 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 several types of sterile stopcocks because the seal on the pouch might be incomplete, which could lead to loss of sterility. This risk is serious for medical use, as it could compromise infection control during procedures.
The seal on the pouch may not form properly, allowing contaminants to enter the sterile product. This could lead to infections during medical procedures if the stopcock is used without a complete seal.
Healthcare professionals and medical facilities using the recalled stopcocks for sterile procedures are most at risk. Patients receiving treatments with these stopcocks could face infection risks.
Check the product label for the model number and lot number. The recalled stopcocks include specific types with lot numbers like 11226656, 11228887, and others listed in the recall notice.
Discontinue use of the recalled stopcocks as they may cause loss of sterility.
The recall includes 6 types of stopcocks with specific model numbers and lot numbers, such as REF 041210002A with lot numbers 11226656 and 11228887.
Look for the model number and lot number on the product label; the recall lists specific lot numbers for each model.
Stop using the stopcock immediately and 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-0290-2020 — Argon Medical Devices Argon Medical Devices Hello, I own a Argon Medical Devices that is covered by recall Z-0290-2020 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.
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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.
