Argon Medical Devices recalls double female and male LL adapters due to incomplete seal risking product sterility. Affected units have specific lot numbers and are sold sterile. 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 two types of sterile adapters because the seal on the pouch might be incomplete, which could cause the product to lose sterility. This means the medical devices might not be safe for use in procedures requiring sterile conditions.
The seal on the pouch edge may not form properly, leading to loss of sterility. This could mean the medical device is no longer safe for procedures that require sterile conditions.
Healthcare professionals and patients using sterile medical adapters for procedures. Those with the specific lot numbers listed are most at risk.
Check the product label for lot numbers: 11228606, 11227966, 11226655 for the female adapter and 11227508, 11229885, 11230268, 11231393 for the male adapter. The adapters are sold sterile and require a prescription.
Look for lot numbers on the adapter packaging: 11228606, 11227966, 11226655 for the female adapter and 11227508, 11229885, 11230268, 11231393 for the male adapter.
Reach out to Argon Medical Devices, Inc. for further instructions on handling the recalled items.
The seal on the pouch edge may be incomplete, which could result in loss of sterility to the product.
Female adapter lot numbers: 11228606, 11227966, 11226655; male adapter lot numbers: 11227508, 11229885, 11230268, 11231393.
The recall indicates a risk of loss of sterility, so they should not be used until the manufacturer provides 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-0288-2020 — Argon Medical Devices Argon Medical Devices Hello, I own a Argon Medical Devices that is covered by recall Z-0288-2020 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.
