Medline recalls sterile barrier packs with improper sterilization due to component placement. Affected items contain BD Chloraprep Hi-Lite Orange. Stop using if you own these specific models.
The convenience trays had improper placement of some of the components that were in the nonsterile portion of the tray, thus, not receiving sterilization.
Medline is recalling sterile surgical packs that may not have been properly sterilized because some components in the nonsterile part weren't sterilized correctly. This could lead to infection risks if used in medical procedures.
The convenience trays in these packs had some components placed incorrectly in the nonsterile section, meaning they didn't receive proper sterilization. This could lead to contamination if the packs are used for medical procedures without being fully sterilized.
Healthcare professionals and medical facilities that use these sterile surgical packs. The risk is low because the issue only affects the nonsterile portion of the pack, not the entire product.
Look for Medline Sterile Maximum Barrier Pack-LF with item numbers DYNJ0248546C or DYNJ0248546D. These packs contain BD Chloraprep Hi-Lite Orange and have specific lot numbers listed in the recall notice.
Identify the item number (DYNJ0248546C or DYNJ0248546D) and lot numbers from the recall list to confirm if your pack is affected.
The convenience trays had improper placement of some components in the nonsterile portion, so they didn't receive full sterilization.
Check the item number and lot numbers to see if it's affected. If it is, stop using it and contact Medline for instructions.
This is a low-risk issue as it only affects the nonsterile portion of the pack, not the entire product.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1162-2023 — Medline Medline Hello, I own a Medline that is covered by recall Z-1162-2023 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.
