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 were sold by Medline.
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 extra raw material on their surface. This could lead to staining and potential harm if the catheter is used.
The catheters have more raw material on their surface than intended. This can cause staining and may be harmful if the raw material is absorbed into the body during use.
Patients using urinary catheters from these specific Medline convenience kits are affected. Healthcare workers who use these kits for patient care are most at risk.
Check for Medline convenience kits with Bard Silastic Foley catheters (French sizes 16, 18, 20) and 5cc balloons. Look for lot numbers 25GBG086, 25JBF391, 25KBA114, 25KBN017, or 25LBQ601.
Identify kits with lot numbers 25GBG086, 25JBF391, 25KBA114, 25KBN017, or 25LBQ601.
The catheters have increased raw material on their surface, which can cause staining and potential harm if used.
Check for lot numbers 25GBG086, 25JBF391, 25KBA114, 25KBN017, or 25LBQ601 on the kit label.
The recall record does not specify a remedy, so contact Medline directly for guidance.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2787-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-2787-2026 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.
