Medline Convenience Kits Recall
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 is recalling 49,654 convenience kits nationwide because they contain a recalled lot of MASTISOL Liquid Adhesive with tubing that may crack.
What this FDA recall tells you, and what most readers miss
This notice was issued by FDA on August 3, 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, Medical Devices.
What Happened
Medline Industries, LP is recalling certain convenience kits that contain a recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. The butyrate tubing may crack during actuation and render the product unusable for application.
Which Products Are Affected
The recall affects the following Medline convenience kits totaling 49,654 units distributed nationwide:
- INPATIENT CENTRAL LN DRSG KIT DYNDC3525 (UDI-DI 10198459576294, Lot 25KBM985)
- PICC/CVC/MIDLINE DRSG CHG KIT DT13191A (UDI-DI 10653160998914, Lot 26AMA168)
- PORT A CATH CDS982047S (UDI-DI 10198459385735, Lot 26AMB202)
- VEIN ABLATION PACK DYNJ62889C (UDI-DI 10198459416453, Lot 26AMA584)
Recall number Z-2419-2026. Distribution is US Nationwide with OUS distribution pending.
What You Should Do
Consumers should contact Medline Industries, LP regarding the recalled kits.
Why This Matters
The affected kits contain adhesive components that may fail during use, potentially impacting medical procedures.
Source
FDA recall Z-2419-2026, report date 20260624.
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 (1,061 characters here).
Similar severity timing
Same severity (medium) notices issued closest in time to August 3, 2026.
Frequently Asked Questions
Common questions about this FDA recall.