Medline recalls non-sterile PVP solution kits with mislabeled sterile packaging. Affected products were incorrectly labeled as 'STERILE PVP SLN' when they should be 'NON-STERILE PVP SOLUTION, STERILE PACKAGING'.
Affected product lots were mislabeled as "STERILE PVP SLN" when they should have been titled "NON-STERILE PVP SOLUTION, STERILE PACKAGING".
Medline is recalling several orthopedic surgery kits that were mislabeled as sterile when they are actually non-sterile. This could lead to infection risks if used in procedures requiring sterile conditions.
The products were incorrectly labeled as 'STERILE PVP SLN' when they should have been 'NON-STERILE PVP SOLUTION, STERILE PACKAGING'. This mislabeling could cause infections if used in procedures requiring sterile conditions, as the non-sterile solution might not be suitable for surgical environments.
Orthopedic surgeons and hospitals using Medline's non-sterile PVP solution kits with the listed model numbers and lot numbers. Patients undergoing surgery with these kits are at risk of infection if the mislabeled products are used in sterile procedures.
Check for model numbers and lot numbers listed in the recall notice. Affected kits include specific orthopedic surgery products with model numbers like CDS985555S, DYNJ0949139I, and others, along with the listed lot numbers.
Look for the model number and lot numbers on the product packaging to determine if it's affected.
The products were mislabeled as sterile when they are non-sterile. Using them in sterile procedures could lead to infection risks.
Check the model number and lot numbers listed in the recall notice. Affected products include specific orthopedic surgery kits with model numbers like CDS985555S, DYNJ0949139I, and others, along with the listed lot numbers.
The recall does not specify a remedy, so contact Medline directly for guidance on handling affected products.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2137-2023 — Medline Medline Hello, I own a Medline that is covered by recall Z-2137-2023 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.
