Medline recalls Ortho Trauma procedural trays that may have sterile blades causing sterile packaging breaches. Stop using if you own these trays.
Potential for sterile blades, within non-sterile SPT kits containing the blades, to puncture the outer foil layer causing a breach in the sterile packaging.
Medline is recalling non-sterile procedural trays labeled as Ortho Trauma because sterile blades inside could puncture the outer foil layer, breaking the sterile packaging. This could lead to infections if used improperly.
Sterile blades inside non-sterile trays can puncture the foil layer, creating a breach in the sterile packaging. This breach could allow contamination if the trays are used without proper sterilization.
Healthcare professionals using these trays in medical settings are most at risk. Patients receiving procedures with these trays could face infection if the packaging is compromised.
Look for trays labeled 'Ortho Trauma' with item number DYNJ908295. Check the case number 40195327029570 or each number 10195327029579. Lot numbers 22IBN449 or 22JBQ931 are also associated with this recall.
Look for trays labeled 'Ortho Trauma' with item number DYNJ908295.
If you have these trays, stop using them immediately to prevent potential contamination.
Sterile blades inside non-sterile trays can puncture the foil layer, causing a breach in the sterile packaging.
Look for trays labeled 'Ortho Trauma' with item number DYNJ908295, case number 40195327029570, or lot numbers 22IBN449 or 22JBQ931.
Stop using them immediately to prevent potential contamination.
We’ve drafted a message you can send Medline Industries to request your refund or repair — edit it as you like.
Subject: Recall Z-1033-2023 — Medline Industries Medline Industries Hello, I own a Medline Industries that is covered by recall Z-1033-2023 from Medline Industries. 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.
