Medline C-SECTION KIT Recall Issued by FDA
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 C-section convenience kits containing a recalled adhesive lot where tubing may crack and render the product unusable.
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, medical-devices.
What Happened
Medline Industries, LP initiated a voluntary recall of certain convenience kits because they 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 Medline convenience kits distributed nationwide in the United States, with OUS distribution pending. Affected products include:
- C-SECTION KIT DYNJ904305J (UDI-DI 10198459268151, lot 25KBT972)
- C-SECTION PACK DYNJ69533C (UDI-DI 10198459524097, lot 26BBC483) A total of 49,654 kits are affected. The FDA recall number is Z-2432-2026 and the classification is Class II.
What You Should Do
The recall is ongoing. Consumers should refer to the FDA recall notice for additional guidance.
Why This Matters
The kits are used in medical procedures and the defect may prevent proper application of the included adhesive.
Source
FDA recall Z-2432-2026 - 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 (1,051 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.