Medline recalls convenience kits containing Bard Silastic Foley Catheters (French sizes 16, 18, 20) due to increased surface raw material causing potential staining and harm. Affected kits have specific lot numbers and UDI codes.
Affected kits contain recalled Bard Silastic Foley Catheters. Catheters were recalled by manufacturer due to increased amount of raw material present on the surface of the catheter. Issue may result in the use of urinary catheters that exhibit staining on the catheter surface; raw material present in increased amounts may be harmful.
Medline is recalling convenience kits that include Bard Silastic Foley Catheters (French sizes 16, 18, 20) because the catheters have more raw material on their surface. This could lead to staining and potential harm from the raw material.
The catheters have increased amounts of raw material on their surface, which may cause staining. This raw material could be harmful if it comes into contact with the body.
Healthcare professionals using these kits for urinary catheter procedures are most at risk. Patients receiving these catheters could be affected if the kits are used.
Check for kits labeled with Bard Silastic Foley Catheters (French sizes 16, 18, 20) and 5cc balloons. Affected kits have specific lot numbers: 25IMC004, 25JMD942, 25JMJ441, 25LMG068.
Look for lot numbers 25IMC004, 25JMD942, 25JMJ441, or 25LMG068 on the kit packaging.
The catheters have increased raw material on their surface, which may cause staining and potential harm.
The recall record does not specify a remedy, so check the kit details to see if it is affected.
Yes, affected kits have lot numbers 25IMC004, 25JMD942, 25JMJ441, or 25LMG068.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2781-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-2781-2026 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.
