Medline recalls two pain kits (DYNJ67577A and DYNJ67576A) due to potential open/weak seals on breather pouches, which could compromise sterility 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 two types of pain kits (PAIN PACK and PAIN TRIAL PACK) because their breather pouches might have weak seals. This could allow contamination during medical procedures if the kits are used improperly.
The breather pouches used to package these kits may have open or weak seals. This could allow unsterile air or contaminants to enter the kit during use, potentially compromising the sterility of medical procedures.
Healthcare professionals using Medline pain kits with model numbers DYNJ67577A or DYNJ67576A are most at risk. Patients receiving these kits may face contamination if the breather pouches are compromised.
Check for model numbers DYNJ67577A (PAIN PACK) or DYNJ67576A (PAIN TRIAL PACK) on the kit packaging. These kits were sold with lot numbers 24JBX252 or 24JBX286.
Identify the model number on the kit packaging to confirm if it is DYNJ67577A or DYNJ67576A.
Reach out to Medline for guidance on whether the kit needs to be discarded or replaced.
The breather pouches used for packaging these kits may have open or weak seals, which could allow contamination during medical procedures.
Model numbers DYNJ67577A (PAIN PACK) and DYNJ67576A (PAIN TRIAL PACK).
Check the model number on the packaging; affected kits have model numbers DYNJ67577A or DYNJ67576A and were sold with lot numbers 24JBX252 or 24JBX286.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1588-2025 — Medline Medline Hello, I own a Medline that is covered by recall Z-1588-2025 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.
