Medline Industries Recalls Cath Lab Packs Over Adhesive Issue
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 49,654 kits containing a recalled lot of MASTISOL Liquid Adhesive where butyrate tubing may crack during use.
What this FDA recall tells you, and what most readers miss
This notice was issued by FDA on August 2, 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
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.
Which Products Are Affected
MINOR CATH LAB PACK DYNJ84775A (UDI-DI 10195327606527, lot 25LMH070) OR VASCULAR ANGIO PACK DYNJ47269D (UDI-DI 10195327674786, lot 25LMJ234) PORT-A-CATH DYNJ63276G (UDI-DI 10198459458835, lot 26BBC598) Total: 49,654 kits. US Nationwide distribution.
What You Should Do
No specific consumer instructions are provided in the recall data.
Why This Matters
This ongoing Class II recall affects medical device kits distributed across the United States.
Source
FDA recall Z-2417-2026, report date 20260624. Attribution: FDA
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 (743 characters here).
Similar severity timing
Same severity (medium) notices issued closest in time to August 2, 2026.
Frequently Asked Questions
Common questions about this FDA recall.