Custom Healthcare Systems recalls UNC-VIR TRAY product UNC-17914 due to improper sterility packaging. Affected units may cause infection if used without proper sterilization.
Convenience kits were sealed in immediate Tyvek pouches using incorrect specifications compromising product sterility
Custom Healthcare Systems is recalling their UNC-VIR TRAY convenience kit (product number UNC-17914) because the packaging was sealed incorrectly, which could compromise sterility. This means the kit might not be sterile when used, increasing infection risk.
The convenience kit was sealed in Tyvek pouches using incorrect specifications, which could compromise the sterility of the product. If the kit is not properly sterilized before use, it may lead to infections.
Healthcare workers and patients using the UNC-VIR TRAY convenience kit for medical procedures. Those with specific medical needs or procedures requiring sterile equipment are most at risk.
Look for the product name 'UNC-VIR TRAY' with product number UNC-17914. The kit was sold with lot number 52418 and expired May 1, 2021.
Verify the product number is UNC-17914 and lot number 52418 to confirm if it's affected.
The recall states the packaging was sealed incorrectly, which could compromise sterility. If not properly sterilized, it may cause infections. Consult your healthcare provider for specific guidance.
The recall record does not mention a replacement or remedy, so no action is required beyond checking if the product is affected.
The product was sold with lot number 52418 and expired May 1, 2021.
We’ve drafted a message you can send Custom Healthcare Systems to request your refund or repair — edit it as you like.
Subject: Recall Z-0262-2019 — Custom Healthcare Systems Custom Healthcare Systems Hello, I own a Custom Healthcare Systems that is covered by recall Z-0262-2019 from Custom Healthcare Systems. 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.
