Medline recalls three convenience kits with potential weak seals on breather pouches that could lead to contamination during medical procedures. Affected kits include ANGIO CONSOLIDATED PACK (DYNJHTCAD1) and others. Consumers should check model numbers and lot dates.
There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.
Medline is recalling three specific convenience kits used in medical procedures because their breather pouches might have weak seals. This could lead to contamination during surgeries or other procedures if the pouches fail to maintain sterility.
The breather pouches used to package the sterile kits may have open or weak seals. If these pouches fail during use, they could allow contaminants to enter the sterile environment, potentially causing infections or contamination of medical instruments.
Healthcare professionals using Medline convenience kits for medical procedures are most at risk. Patients undergoing surgeries or procedures with these kits could face contamination if the breather pouches fail.
Check for model numbers: DYNJHTCAD1 (Angio Consolidated Pack), DYNJ05350V (Angiography Tray-LF), or DYNJ38144C (Angiography Pack). Lot numbers 24JBS743, 24JBU500, or 24KBD294 indicate affected units.
Identify the model number on the kit to see if it matches DYNJHTCAD1, DYNJ05350V, or DYNJ38144C.
Confirm the lot number is 24JBS743, 24JBU500, or 24KBD294 to determine if the kit is affected.
The breather pouches used to package these kits may have open or weak seals, which could lead to contamination during medical procedures.
Check the model number and lot number to see if your kit is affected. If it is, contact Medline for further instructions.
If the breather pouches fail, they could allow contaminants to enter the sterile environment, potentially causing infections or contamination of medical instruments.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1590-2025 — Medline Medline Hello, I own a Medline that is covered by recall Z-1590-2025 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.
