Medline recalls 170 specific breather pouch models used in sterile medical kits due to potential open or weak seals that could compromise sterility.
There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.
Medline is recalling 170 specific breather pouch models used for packaging sterile medical kits because they may have open or weak seals. This could allow contamination of the sterile kits if the pouches are used improperly.
The breather pouches used for packaging sterile medical kits may have open or weak seals. This could allow contamination of the sterile kits if the pouches are not properly sealed or if the kits are exposed to air during use.
Healthcare professionals and medical facilities that use Medline's sterile kits with the recalled breather pouches are most at risk. The recall applies to specific models sold with certain lot numbers.
Check the product model number (e.g., DYNJHTLD02A, DYNJ50017B) and lot number (e.g., 24IBE784) on the pouch. The recall includes 170 specific models with specific lot numbers listed in the recall notice.
Look for the model number (e.g., DYNJHTLD02A) and lot number (e.g., 24IBE784) on the breather pouch.
The breather pouches may have open or weak seals that could compromise sterility of the sterile medical kits they package.
Check the model number and lot number on the pouch. The recall includes 170 specific models with specific lot numbers listed in the notice.
The recall does not specify a remedy, so no action is required if you have the pouch. However, you should check if it's affected before using the sterile kit.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1602-2025 — Medline Medline Hello, I own a Medline that is covered by recall Z-1602-2025 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.
