Medline Convenience Kits Containing Bard Silastic Foley Catheters Recalled Due to Surface Material Issues
Medline Industries, LP is recalling 980 Medline convenience kits containing Bard Silastic Foley Catheters because excess raw material on the catheter surface may be harmful.
What this means for you
Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.
Our severity reasoning: The product is a medical device with a potential for harm due to material contamination, but no injuries or illnesses have been reported in the source text.
Plain-English summary
Medline Industries, LP is recalling 980 Medline convenience kits that contain Bard Silastic Foley Catheters (French sizes 16, 18, 20) with 5cc balloons. The affected kits include lot numbers 25KBJ177, 25LBO527, and 26ABT761.
The manufacturer issued the recall because an increased amount of raw material was found on the surface of the catheters. This issue may cause the catheters to exhibit staining on the surface, and the excess raw material may be harmful to users.
These kits were distributed nationwide in the United States, specifically in California, Florida, Maryland, Pennsylvania, and Texas. Users should check their inventory for the affected lot numbers.
The recalled product
- Product
- Medline convenience kits containing Bard¿ Silastic¿ Foley Catheters (French sizes 16, 18, 20) 5cc balloons. ROBOTIC CDS980523M
- Manufacturer
- Medline Industries, LP
- Hazard
- material-contamination
- potential-harm
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (1)
- CDS980523M UDI-DI 10195327508913 Lots 25KBJ177 25LBO527 26ABT761
Distribution
Distributed nationwide across the United States.
Related recalls
Same category
- HighHalyard STANDARD LINE INSERTION PACK Recall for Silicone Seal Defect
FDA (Devices) · 2026-07-29
- SevereMEDLINE Medical Procedure Kits Containing Bupivacaine Recalled Due to Drug Ineffectiveness
FDA (Devices) · 2026-07-29
- HighFARADRIVE STEERABLE SHEATH CLEAR Medical Device Recall
FDA (Devices) · 2026-07-29
- HighBoston Scientific Recalls FARASTAR Ablation Generators Due to Catheter Incompatibility
FDA (Devices) · 2026-07-29
- HighPenumbra System RED 68 Reperfusion Catheter Recall Due to Fracture Risk
FDA (Devices) · 2026-07-29