Medline recalls 12 types of C-section convenience kits due to 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 12 different C-section convenience kits because the breather pouches used to package them might have weak seals. This could lead to contamination during medical procedures if the pouches are not properly sealed.
The breather pouches that package the sterile convenience kits may have open or weak seals. If these pouches are not properly sealed, they could allow contaminants to enter the sterile environment during medical procedures.
Healthcare professionals using these kits in emergency settings are most at risk. Patients undergoing C-section procedures with these kits could be exposed to contamination.
Check for model numbers: MNS13635A, DYNJ81281, OBK387M, DYNJ40573A, CDS983998C, DYNJ64300A, DYNJ55205, DYNJ56550, DYNJ83507, DYNJ83248, and DYNJ81281. These kits were sold with specific lot numbers between 24IBH747 and 24KBG874.
Identify the model number on the kit packaging to determine if it is recalled.
Reach out to Medline for assistance with the recall if you have the kit.
The recall states there is a potential for weak seals on breather pouches, but the kits are not unsafe to use if the pouches are properly sealed.
Check the model number on the kit packaging. Recalled kits include MNS13635A, DYNJ81281, OBK387M, DYNJ40573A, CDS983998C, DYNJ64300A, DYNJ55205, DYNJ56550, DYNJ83507, DYNJ83248, and DYNJ81281 with specific lot numbers between 24IBH747 and 24KBG874.
Contact Medline directly for assistance with the recall. They will provide guidance on next steps.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1614-2025 — Medline Medline Hello, I own a Medline that is covered by recall Z-1614-2025 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.
