Medline recalls convenience kits with Bard Silastic Foley catheters (French sizes 16, 18, 20) due to surface material that may cause staining and potential harm. Affected kits have specific lot numbers and were sold with certain medical procedures.
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 contain Bard Silastic Foley catheters (French sizes 16, 18, 20) because the catheters have extra raw material on their surface. This could lead to staining and potential harm if used.
The catheters have increased raw material on their surface, which can cause staining. This raw material may be harmful if it comes into contact with the body during use.
Healthcare professionals who use Medline convenience kits with Bard Silastic Foley catheters (French sizes 16, 18, 20) are likely affected. Patients receiving these catheters may be at risk if the catheters cause staining or harm.
Check for Medline convenience kits with Bard Silastic Foley catheters (French sizes 16, 18, 20) 5cc balloons. Affected kits have lot numbers 25IMF461 or 25LMG907 and were sold with specific medical procedures like laparoscopic prostate procedures.
Look for lot numbers 25IMF461 or 25LMG907 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 with Medline for guidance.
Yes, affected kits have lot numbers 25IMF461 or 25LMG907.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2786-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-2786-2026 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.
