Medline recalls 16 types of sterile convenience kits with potential weak seals on breather pouches that could lead to contamination during medical procedures.
There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.
Medline is recalling 16 different sterile convenience kits used in medical procedures because some breather pouches may have weak seals. This could allow contamination during procedures if the pouches are not properly sealed.
The breather pouches used to package some sterile kits may have open or weak seals. This could allow contaminants to enter the sterile environment during medical procedures, potentially causing infections.
Healthcare professionals who use these kits for procedures like line insertions or PICC lines are most at risk. Patients receiving procedures using these kits could be affected if the seals fail.
Check for model numbers listed in the recall: DYNJ44949C, DYNJ41682C, DYNJ81267A, DYNJ82437A, CDS980379J, DYNJ24529M, DYNJ65827, DYNJ55170F, PHS902533005, DYNDH1904, DYNJ55356A, DYNJ15652M, DYNJ80643, DYNJ20803D. These kits were sold with specific lot numbers from 2024.
Look for model numbers on the kit packaging: DYNJ44949C, DYNJ41682C, DYNJ81267A, DYNJ82437A, CDS980379J, DYNJ24529M, DYNJ65827, DYNJ55170F, PHS902533005, DYNDH1904, DYNJ55356A, DYNJ15652M, DYNJ80643, DYNJ20803D.
The recall does not require immediate stop use; the hazard is low risk and the remedy is not specified.
The official notice does not specify a remedy, so contact Medline directly for guidance.
Yes, the kits were sold with specific lot numbers from 2024, but the exact lot numbers are not provided in the recall notice.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1593-2025 — Medline Medline Hello, I own a Medline that is covered by recall Z-1593-2025 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.
