Medline recalls non-sterile PVP solution with sterile packaging due to mislabeling. This could lead to incorrect use in medical settings. Affected lots include specific batch numbers from January 2023.
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 that was mislabeled as sterile. Using this product in medical procedures could cause infections or improper treatment because it's not sterile.
The product was mislabeled as 'sterile' when it's actually non-sterile. This means it could cause infections or improper medical procedures if used in sterile environments like surgeries or wound care.
Healthcare professionals using this product in medical settings. Those handling the product without verifying the label are at risk of using non-sterile solution where sterile is required.
Check for the product name 'Medline Non-sterile PVP Solution, Sterile Packaging' with the reference code DYNDA2232A. Look for batch numbers: 2023011090, 2023011190, 2023011790, 2023012090, 2023012590, 2023020790, 2023022390, or 2023022490.
Look for the batch numbers listed in the recall: 2023011090, 2023011190, 2023011790, 2023012090, 2023012590, 2023020790, 2023022390, or 2023022490.
No, using this product in sterile medical procedures could cause infections or improper treatment because it's mislabeled as sterile when it's non-sterile.
The recall does not specify a remedy, so check the product label for batch numbers and contact Medline for guidance if needed.
Look for the product name 'Medline Non-sterile PVP Solution, Sterile Packaging' with reference code DYNDA2232A and batch numbers listed above.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2131-2023 — Medline Medline Hello, I own a Medline that is covered by recall Z-2131-2023 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.
