Medline Convenience Kits Recall
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Medline Industries, LP is recalling 49,654 convenience kits containing recalled MASTISOL Liquid Adhesive because butyrate tubing may crack during actuation.
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, Devices.
What Happened
Medline Industries, LP initiated a voluntary recall of 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 covers two Medline convenience kits distributed nationwide in the United States:
- ADD-A-CATH ARTERIAL INSERTION (ARTNC185), UDI-DI 10195327640729, Lot 25JBU463
- PED SCHOOL AGE PICC DRSG TRAY (DYNDC3291), UDI-DI 10195327334741, Lot 25KBH082 A total of 49,654 kits are affected under recall number Z-2445-2026. Distribution outside the United States is pending.
What You Should Do
Consumers should follow instructions provided by the recalling firm regarding the affected kits.
Why This Matters
The recall addresses a defect that could prevent proper use of the kits in medical procedures.
Source
FDA recall number Z-2445-2026, Class II, event ID 98951.
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 (980 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.