Medline recalls URINALYSIS KIT 4 (SKU DYLAB102: Component No. 503581) due to non-sterile specimen containers that may cause unnecessary treatment or hospitalization. Affected lots: 22FBK384, 22GBO520.
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 URINALYSIS KIT 4 (SKU DYLAB1021) because the specimen container is labeled as sterile but is actually non-sterile. This could lead to unnecessary treatments or longer hospital stays if used improperly.
The specimen container in the kit is marked as sterile but has been found to be non-sterile. This means it could introduce contaminants into urine samples, potentially leading to unnecessary treatments or extended hospital stays if the contamination causes infections.
People who purchased or use the URINALYSIS KIT 4 (SKU DYLAB1021) with lots 22FBK384 or 22GBO520. Healthcare providers using these kits for urine tests are most at risk.
Check for the kit's SKU DYLAB1021, Component No. 503581, and lots 22FBK384 or 22GBO520. The kit is sold by Medline Industries in Northfield.
Look for lot numbers 22FBK384 or 22GBO520 on the kit's packaging or label.
The kit is not safe for use as the specimen container is non-sterile, which could lead to unnecessary treatments or hospitalization.
The recall record does not specify a remedy, so contact Medline Industries for guidance.
Check for SKU DYLAB1021, Component No. 503581, and lots 22FBK384 or 22GBO520.
We’ve drafted a message you can send Medline Industries to request your refund or repair — edit it as you like.
Subject: Recall Z-0357-2025 — Medline Industries Medline Industries Hello, I own a Medline Industries that is covered by recall Z-0357-2025 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.
