Medline recalls sterile oncology port access trays with improper sterilization due to component placement. Affected items include specific model #DYNDC2239 with certain lot numbers. Consumers should check their product details and contact Medline for guidance.
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 oncology port access trays that may not have been properly sterilized because some components were misplaced in the nonsterile section. This could lead to infections if used in medical procedures without proper sterilization.
The trays have components that weren't properly sterilized because they were placed in the nonsterile section of the tray. This means the trays might not be safe for medical use, increasing infection risk during procedures.
Healthcare professionals using these trays for oncology procedures are most at risk. Patients receiving treatments with these trays could face infection if the trays weren't fully sterilized.
Check for the model number DYNDC2239 on the tray. Look for lot numbers listed in the recall: 22OBD978 through 22ABK594 with specific expiration dates.
Identify the model number DYNDC2239 and lot numbers listed in the recall notice.
The trays may not have been properly sterilized because some components were misplaced in the nonsterile section, increasing infection risk during medical procedures.
Check for model number DYNDC2239 and lot numbers listed: 22OBD978 through 22ABK594 with specific expiration dates.
The recall does not specify a remedy, so contact Medline directly for guidance on next steps.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1161-2023 — Medline Medline Hello, I own a Medline that is covered by recall Z-1161-2023 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.
