Medline recalls NAMIC Cath Lab kits (Model #650600111) sold without sterilization capabilities. Kits intended for sterile use were sold to hospitals lacking sterilization equipment, risking infection.
Non-sterile kits intended to be sterilized prior to use were sold to accounts without sterilization capabilities.
Medline is recalling NAMIC Cath Lab kits that were sold to hospitals without sterilization capabilities. These kits are meant to be sterilized before use but were sold to facilities that can't properly sterilize them, increasing infection risk.
The kits are designed to be sterilized before use but were sold to hospitals that lack the necessary sterilization equipment. This means the kits could become contaminated and cause infections if used without proper sterilization.
Hospitals and medical facilities that purchased these kits for catheter labs or interventional radiology procedures. Staff using the kits without proper sterilization are at risk of infection.
Check for the model number 650600111 on the kit. These kits were sold to hospitals like St. Francis Hospital for cardiac catheter labs and interventional radiology procedures between the dates listed in the product description.
Look for the model number 650600111 on the kit packaging or label.
The kits were sold to hospitals without sterilization capabilities, but they are designed to be sterilized before use, increasing infection risk.
No, these kits are not safe to use without proper sterilization, which hospitals that purchased them may not have.
The recall record does not specify a remedy, so hospitals should contact Medline directly for guidance.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-0066-2021 — Medline Medline Hello, I own a Medline that is covered by recall Z-0066-2021 from Medline. 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.
