Medline Convenience Kits Recall Due to Adhesive Tubing Issue
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Medline Industries, LP is recalling 49,654 convenience kits distributed nationwide because they contain a recalled lot of MASTISOL Liquid Adhesive with butyrate 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 initiated a voluntary recall of certain convenience kits containing 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 49,654 kits total with US Nationwide distribution. Affected products include:
- BREAST IMAGING DYNJT5893 (UDI-DI 10198459517839, Lot 25KBA123)
- CHOG PLASTICS SYNJ10306A (UDI-DI 10193489296891, Lots 25LBO305, 26CBD081)
- ENDO BREAST AUGMENTATION PACK DYNJ68023 (UDI-DI 10193489468083, Lot 25KBI169)
- FACIAL PLASTIC DYNJ909926C (UDI-DI 10198459423109, Lots 25LBC067, 25LBR659)
- And additional kits: DYNJ84081B, DYNJ905362C, DYNJ0660040R, DYNJ89023A, DYNJ902510M, DYNJ84766, DYNJ0578842M, DYNJ63803C, DYNJ62433D, DYNJ81772C, DYNJT7588, DYNJ89048A with listed lots. Recall number Z-2423-2026, Class II, initiated April 27, 2026.
What You Should Do
Consumers should contact Medline Industries, LP regarding the recalled kits.
Why This Matters
This Class II recall involves products that may become unusable due to a component defect in kits distributed across the United States.
Source
FDA recall Z-2423-2026, Medline Industries, LP, Northfield, IL.
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 (1,261 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.