MEDLINE recalls non-sterile PVP solution kits (Model DYNJ902348L) that were mislabeled as sterile. This could lead to infection risks if used in medical procedures.
Affected product lots were mislabeled as "STERILE PVP SLN" when they should have been titled "NON-STERILE PVP SOLUTION, STERILE PACKAGING".
MEDLINE is recalling non-sterile PVP solution kits that were incorrectly labeled as sterile. Using these kits in medical procedures could cause infections because they are not sterile.
The kits were mislabeled as sterile when they are actually non-sterile. This means they cannot be used safely in medical procedures that require sterile conditions, increasing infection risk.
Healthcare workers using these kits in medical procedures are most at risk. Patients receiving treatments with these kits could face infection risks.
Check for the model number DYNJ902348L on the kit. The lot numbers 23EDA775 and 23CDB962 are also associated with this recall.
Look for the model number DYNJ902348L and lot numbers 23EDA775 or 23CDB962 on the kit.
The product was mislabeled as sterile when it is actually non-sterile, which could lead to infection risks in medical procedures.
Check the product label for the model number DYNJ902348L and lot numbers 23EDA775 or 23CDB962. If you have these, contact MEDLINE for guidance.
The recall record does not mention a remedy, so no specific fix is provided.
We’ve drafted a message you can send MEDLINE to request your refund or repair — edit it as you like.
Subject: Recall Z-2134-2023 — MEDLINE MEDLINE Hello, I own a MEDLINE that is covered by recall Z-2134-2023 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.
