Medline recalls urine test kits with non-sterile specimen containers that may cause unnecessary treatment or hospitalization. Affected kits include SKU DYLAB1001A with specific lot numbers.
Specimen container included in kits is labeled as sterile, but has been identified to be non-sterile. Long-term consequences may include unnecessary treatment and/or prolonged hospitalization.
Medline is recalling urine test kits that contain non-sterile specimen cups. Using these kits could lead to unnecessary medical treatment or longer hospital stays due to contamination.
The specimen container is labeled as sterile but has been found to be non-sterile. This can lead to contamination of the urine sample, potentially causing infections that require unnecessary medical treatment or extended hospital stays.
People who purchased the affected urine test kits from the listed lot numbers. Those using the kits for home testing are most at risk if they have a compromised immune system.
Check for the SKU DYLAB1001A and lot numbers 22DBP031 (case) or 22DBP031 (each) on the kit packaging. The product was sold with UDI/DI numbers 40193489383707 and 10193489383706.
Look for SKU DYLAB1001A and lot numbers 22DBP031 (case) or 22DBP031 (each) on the product label.
The specimen container is labeled as sterile but has been identified as non-sterile, which may lead to unnecessary treatment or prolonged hospitalization.
The recall record does not specify a remedy, so check the kit packaging for the lot numbers and contact Medline for further instructions.
The recall states long-term consequences like unnecessary treatment or hospitalization, but does not mention immediate injury risks.
We’ve drafted a message you can send Medline Industries to request your refund or repair — edit it as you like.
Subject: Recall Z-0361-2025 — Medline Industries Medline Industries Hello, I own a Medline Industries that is covered by recall Z-0361-2025 from Medline Industries. 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.
