Medline recalls two convenience kits for procedures due to reports of shorter skin barrier protection time. Affected kits may need replacement to prevent skin injury during use.
Kits contain recalled components due to reports of reduced skin barrier wear time. This refers to a shorter duration that a skin barrier can effectively adhere to and protect the skin before it needs to be replaced.
Medline is recalling adult intubation trays and main dispense kits for procedures because they contain components that can cause skin barriers to wear out faster than intended. This means the skin protection might not last as long, increasing the risk of skin injury during medical procedures.
The kits contain components that reduce how long a skin barrier can protect the skin before it needs replacement. This means the skin barrier might not last as long as intended, potentially leading to skin injury during medical procedures.
Healthcare professionals using Medline convenience kits for procedures are most at risk. Patients receiving these kits during medical procedures could also be affected if the skin barrier wears out too quickly.
Check for model numbers DYNJAA254A or DYNJAA262A on the kits. The lot numbers 24KBR956, 24LBA655 for the first kit and 24LBD397 for the second kit are also indicators of affected units.
Look for model numbers DYNJAA254A or DYNJAA262A on the kits.
The recall is due to reports that the kits contain components causing skin barriers to wear out faster than intended.
The official notice does not specify a remedy, so check with Medline for further instructions.
Affected kits have model numbers DYNJAA254A or DYNJAA262A and lot numbers 24KBR956, 24LBA655 or 24LBD397.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1182-2025 — Medline Medline Hello, I own a Medline that is covered by recall Z-1182-2025 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.
