Medline recalls Clean Catch Kit (SKU DYKM1833A) due to non-sterile specimen container that may cause unnecessary treatment or hospitalization. Affected lots listed in recall.
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 Clean Catch Kits with non-sterile specimen containers that could lead to unnecessary medical treatment or hospital stays. This affects kits sold with specific lot numbers.
The specimen container in the kit is labeled as sterile but has been found to be non-sterile. This could lead to infections or require additional medical treatment if used improperly.
People who own or use Medline Clean Catch Kits with the specified lot numbers may be affected. Those using the kits for medical purposes are most at risk.
Check the kit's lot number on the packaging. Affected lots include 19LAA531, 20BAA260, 21KBJ974, 22JBK243, 22LBJ966, 23BBU789, 23FBN998, 23HBW916, 23IBH024, 24CBE580, 24DBT234, 24GBA986, and 24GBL321.
Look for the lot number on the packaging to determine if your kit is affected.
The specimen container is non-sterile, which may lead to unnecessary treatment or hospitalization. Do not use affected kits.
Check the lot number on the packaging. If it matches the listed lots, stop using the kit and contact Medline for instructions.
Affected kits have specific lot numbers: 19LAA531, 20BAA260, 21KBJ974, 22JBK243, 22LBJ966, 23BBU789, 23FBN998, 23HBW916, 23IBH024, 24CBE580, 24DBT234, 24GBA986, and 24GBL321.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-0354-2025 — Medline Medline Hello, I own a Medline that is covered by recall Z-0354-2025 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.
