Medline recalls sterile hand packs with improper sterilization due to component placement. Affected items include specific model numbers and expiration dates. Consumers should check their packs for the listed lot numbers.
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 hand packs that may not have been properly sterilized because some components in the nonsterile part of the tray weren't sterilized. This could lead to infections if used in medical procedures. Affected products include specific model numbers and expiration dates.
The convenience trays had components in the nonsterile portion that didn't receive proper sterilization. This means the packs might not be sterile when used, increasing infection risk during medical procedures.
Healthcare workers using Medline sterile hand packs for medical procedures are most at risk. Patients receiving procedures with these packs could be exposed to infection.
Check for model numbers DYNJ63380A or DYNJ63380C with specific lot numbers listed in the recall notice. The packs contain BD Chloraprep Hi-Lite Orange, 26 mL applicators.
Look for model numbers DYNJ63380A or DYNJ63380C with the listed lot numbers on the packaging.
The convenience trays had improper placement of some components in the nonsterile portion, so they weren't sterilized properly.
Check the product details for the model numbers and lot numbers listed in the recall notice. If they match, stop using it.
Yes, the packs may not be sterile, which could lead to infections during medical procedures.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1163-2023 — Medline Medline Hello, I own a Medline that is covered by recall Z-1163-2023 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.
