Medline Convenience Kits Recall Due to Foley Catheters
Areazine synthesizes this FDA recall directly from FDA's official public data feed. See our methodology for full source attribution and refresh cadence.
Medline Industries, LP is recalling 980 kits containing Bard Silastic Foley Catheters due to increased raw material on the catheter surface that may be harmful.
What this FDA recall tells you, and what most readers miss
This notice was issued by FDA on August 12, 2026 and geographically references United States. Its severity classification of "medium" signals how the issuing agency weighs the risk of harm if no action is taken - "critical" and "high" tier alerts typically carry direct consumer actions, while "medium" and "low" tend toward informational guidance or monitoring advisories. The category it belongs to - FDA Recalls - determines the consumer-protection framework behind it, which shapes what remedies (refunds, replacements, repairs, or the recall itself) are available to affected consumers and which agency holds statutory responsibility for enforcement.
Most readers skim a notice like this, check whether they are personally affected, and move on. The more useful lens is to verify its scope, source, and timestamp, then compare related notices without assuming that one record proves a broader trend.
Areazine pairs this record with the original agency URL so you can check the primary source before acting. Its related labels are recall, product-safety, fda, MedicalDevices.
What Happened
Medline Industries, LP initiated a voluntary recall of convenience kits because they contain recalled Bard Silastic Foley Catheters. The catheters were recalled by the manufacturer due to an increased amount of raw material present on the surface, which may result in staining and may be harmful.
Which Products Are Affected
Medline convenience kits containing Bard® Silastic® Foley Catheters (French sizes 16, 18, 20) 5cc balloons. The affected product is KIT ROBOTICS UROLOGY PROSTATE DYKMBNDL116I with UDI-DI 10198459644764 and lots 26ABL226 and 26BBD710. A total of 980 kits are affected. Distribution was limited to the states of CA, FL, MD, PA, and TX.
What You Should Do
No specific consumer action steps are provided in the recall notice.
Why This Matters
This Class II recall involves devices that may cause temporary or reversible adverse health consequences due to potential exposure to excess raw material.
Source
FDA recall number Z-2779-2026, event ID 99301.
Original source: FDA Official Notice ↗
Related FDA Recalls
All FDA Recalls →Nationwide notices with similar length or severity timing 8
Two Areazine-derived peer sets for this FDA recall: nearest notices by body length and by same severity near the same agency date. Peers come from other categories so they are not the same-feed Related list above.
Similar body length
Nearest notices by article body length (1,005 characters here).
Similar severity timing
Same severity (medium) notices issued closest in time to August 12, 2026.
Frequently Asked Questions
Common questions about this FDA recall.