Argon Medical Devices recalls sterile AHD Luer Lock Caps (REF 501303) due to potential incomplete pouch seals risking product sterility. Affected lots 11228902 and 1123044: stop using immediately.
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 AHD Luer Lock Caps (REF 501303) because the pouch seal might be incomplete, which could cause contamination. This affects medical use where sterility is critical, so users should stop using the product immediately.
The pouch seal on the cap may not form properly, allowing contaminants to enter the sterile product. This could lead to infections or complications during medical procedures if the cap is used without sterility.
Healthcare professionals and medical facilities using the sterile caps for procedures. Those handling the specific lots (11228902 and 11230445) are most at risk.
Check for the product name 'Argon Medical Devices AHD Luer Lock Cap', reference number REF 501303, and sterile packaging. Affected lots are 11228902 and 11230445.
Discard the affected caps as they may not be sterile and could cause infections during medical procedures.
The seal on the pouch may be incomplete, which could result in a loss of sterility to the product.
Lots 11228902 and 11230445.
Look for the product name 'Argon Medical Devices AHD Luer Lock Cap', reference number REF 501303, and sterile packaging. Affected lots are 11228902 and 11230445.
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-0296-2020 — Argon Medical Devices Argon Medical Devices Hello, I own a Argon Medical Devices that is covered by recall Z-0296-2020 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.
