MEDLINE recalls pain tray surgical kits with non-sterile outer wrapping. Only inner contents are sterile, risking infection during procedures.
The recall is due to the perforated bag not allowing for outside of the kit wrapping to be sterile, therefore, only the contents inside the kits wrapping are sterile.
MEDLINE is recalling surgical pain tray kits because the outer wrapping isn't sterile. This means the entire kit could become contaminated during use, increasing infection risk for patients.
The perforated bag allows contaminants to enter the outer wrapping. Only the contents inside the kit's inner wrapping are sterile, so the entire kit may not be safe for surgical use.
Healthcare professionals using these kits in medical settings. Patients undergoing procedures are at risk if the kit is used without proper sterility.
Look for kits labeled 'MEDLINE PAIN TRAY' with reorder number DYNJRA1122A. They have GTIN 10193489720594 and lot number 22EBA798.
Verify the kit label for 'MEDLINE PAIN TRAY' and reorder number DYNJRA1122A.
The perforated bag doesn't keep the outer wrapping sterile, so only the inner contents are sterile.
Yes, because the entire kit could become contaminated during use, increasing infection risk.
Look for kits labeled 'MEDLINE PAIN TRAY' with reorder number DYNJRA1122A, GTIN 10193489720594, and lot number 22EBA798.
We’ve drafted a message you can send MEDLINE to request your refund or repair — edit it as you like.
Subject: Recall Z-1109-2023 — MEDLINE MEDLINE Hello, I own a MEDLINE that is covered by recall Z-1109-2023 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.
