Medline recalls urine collection kits with non-sterile specimen containers that may cause unnecessary treatment and hospitalization. Affected kits have specific SKUs and 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 collection kits because the specimen containers are labeled as sterile but are actually non-sterile. This could lead to unnecessary medical treatments or longer hospital stays if used improperly.
The specimen containers in the kits are labeled as sterile but have been found to be non-sterile. This means they could introduce bacteria or contaminants into urine samples, potentially causing infections that require additional medical treatment or extended hospital stays.
People who own or use Medline urine collection kits with the specific SKU DYLAB1016 and lot numbers 22HLA350 or 22HLB291 are affected. Those using these kits for medical purposes are at higher risk of complications.
Check for the SKU DYLAB1016 on the kit and lot numbers 22HLA350 or 22HLB291. The kits were sold with UDI/DI codes 40195327139941 (case) and 10195327139940 (each).
Verify the SKU DYLAB1016 and lot numbers 22HLA350 or 22HLB291 on the kit packaging.
The specimen containers are labeled as sterile but have been identified as non-sterile, which could lead to unnecessary medical treatments or prolonged hospitalization.
The recall record does not specify a remedy, so no action is required beyond checking if your kit matches the described details.
Yes, non-sterile containers could introduce contaminants, potentially causing infections that may require additional treatment or extended hospital stays.
We’ve drafted a message you can send Medline Industries to request your refund or repair — edit it as you like.
Subject: Recall Z-0359-2025 — Medline Industries Medline Industries Hello, I own a Medline Industries that is covered by recall Z-0359-2025 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.
