Medline recalls sterile convenience kits that may not have been properly sterilized, posing infection risks. Affected kits include Extremity Pack model DYNJ4570: 25GBF686 lot.
Convenience kits labeled as sterile have not gone through the sterilization process.
Medline is recalling sterile convenience kits that may not have gone through sterilization. Using these kits could lead to infections since they're not properly sterilized.
These kits are labeled as sterile but have not completed the sterilization process. Without proper sterilization, they can carry harmful bacteria and cause infections when used.
Users of sterile medical kits, especially those in healthcare settings. Patients and medical staff using these kits without proper sterilization are at risk of infection.
Check for the model number DYNJ45701B on the kit. The lot number 25GBF686 is associated with this recall. These kits were sold with the UDI-DI numbers 10193489856279 and 40193489856270.
Look for the model number DYNJ45701B and lot number 25GBF686 on the kit.
No, these kits may not have been properly sterilized and could cause infections.
The recall does not specify a remedy, so check with Medline for further instructions.
Look for the model number DYNJ45701B and lot number 25GBF686 on the kit.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2593-2025 — Medline Medline Hello, I own a Medline that is covered by recall Z-2593-2025 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.
