Medline recalls convenience kits with potential weak seals on breather pouches that could lead to contamination during medical procedures. Affected kits include PRECIP TRAY model MNS12590.
There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.
Medline is recalling convenience kits used in medical procedures because the breather pouches might have weak seals. This could lead to contamination if the pouches are not properly sealed during use.
The breather pouches used to package sterile convenience kits may have open or weak seals. This could allow contaminants to enter the kit during use, potentially leading to infections if the pouches are not properly sealed.
Healthcare professionals using Medline convenience kits, especially those handling sterile procedures. The risk is low as the hazard involves potential contamination rather than immediate injury.
Check for the model number MNS12590 on the kit. The kits were sold with lot numbers starting with 24IBH166. This recall applies to specific convenience kits used in medical procedures.
Look for the model number MNS12590 on the kit packaging or label.
The breather pouches used to package the convenience kits may have open or weak seals, which could lead to contamination during medical procedures.
Check the model number on the kit. If it's MNS12590, contact Medline for further instructions.
The recall addresses potential contamination risk, not direct injury. The hazard level is low risk as it involves contamination rather than immediate harm.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1603-2025 — Medline Medline Hello, I own a Medline that is covered by recall Z-1603-2025 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.
