Custom Healthcare Systems recalls CHS Custom Convenience Kit-LP needles (Product NC401000) due to improper sterility packaging. Affected units may pose infection risks 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 CHS Custom Convenience Kit-LP needles (Product Number NC401000) because the packaging was sealed with incorrect specifications, which could compromise the sterility of the needles. This means the needles might not be sterile when used, increasing the risk of infection during medical procedures.
The needles were sealed in Tyvek pouches using incorrect specifications, which could compromise the sterility of the product. If the needles are not properly sterilized before use, they might introduce infections during medical procedures.
Healthcare professionals who use these needles for medical procedures are most at risk. Patients receiving procedures with these needles could face infection risks if the needles are not properly sterilized.
Check for Product Number NC401000 on the packaging. The lot number is 51018 and the expiration date is May 1, 2021. This product was sold between 2020 and 2021.
Look for Product Number NC401000 on the packaging, Lot number 51018, and Expiration Date May 1, 2021.
The recall indicates the packaging may not have maintained sterility, so these needles should not be used without proper sterilization.
Check for Product Number NC401000 on the packaging, Lot number 51018, and Expiration Date May 1, 2021.
The recall does not specify a remedy, so contact Custom Healthcare Systems for guidance on safe handling.
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-0251-2019 — Custom Healthcare Systems Custom Healthcare Systems Hello, I own a Custom Healthcare Systems that is covered by recall Z-0251-2019 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.
