Medline recalls 20 convenience kits for medical procedures due to potential weak seals on breather pouches that could lead to contamination. Affected kits include Angiography Drape Packs and others with specific 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 20 different convenience kits used in medical procedures because some breather pouches might have weak seals. This could lead to contamination of sterile kits during use, posing a risk to patient safety.
The breather pouches used to package some sterile medical kits may have open or weak seals. This could allow contaminants to enter the kit during use, potentially leading to infections or other complications for patients.
Healthcare professionals and medical facilities that use these convenience kits for procedures like angiography or radiology are most at risk. Patients using these kits could be exposed to contamination if the seals fail.
Check for model numbers listed in the recall: HCP075G, DYNJ64354A, 0M-CP01029D, DYNJ81454B, DYNJ51338C, DYNDH1228, DYNJ83961A, DYNJ85070, DYNJ39515A, 00-398650AJ, DYNJ24812D, DYNJ69974, DYNJ69135A, DYNJ45020, DYNJ51240A, DYNJ43969, DYNJ41932I, 0M-CP01029D, DYNJ81454B. These kits were sold with specific lot numbers from 2024.
Look for model numbers like HCP075G, DYNJ64354A, or 0M-CP01029D on the kit packaging.
The breather pouches used to package some sterile medical kits may have open or weak seals, which could allow contaminants to enter the kit during use.
These kits are used for procedures like angiography, radiology, and interventional radiology.
Check the model number on the kit packaging; affected kits include specific models listed in the recall with lot numbers from 2024.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1591-2025 — Medline Medline Hello, I own a Medline that is covered by recall Z-1591-2025 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.
