Medline recalls non-sterile PVP solution kits (Model DYNJ908683A) 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 lead to infections if the solution is not properly sterilized.
The kits were mislabeled as 'sterile' when they are actually non-sterile. This means the solution could not be properly sterilized and might cause infections if used in medical procedures.
Healthcare professionals using Medline's non-sterile PVP solution kits for medical procedures may be affected. Those handling the kits without verifying the label could face infection risks.
Check for Model Number DYNJ908683A on the kit. The lot number is 23DDA761. The product was sold with a UDI/DI code of 10159327251772 or 40195327251773.
Check the label for the model number DYNJ908683A and lot number 23DDA761.
The product was mislabeled as 'sterile' when it is actually non-sterile, which could lead to infection risks if used in medical procedures.
Check the label for model number DYNJ908683A and lot number 23DDA761. If you have the product, verify it is not sterile before use.
The recall record does not mention a remedy or fix for this issue.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2133-2023 — Medline Medline Hello, I own a Medline that is covered by recall Z-2133-2023 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.