Medline C-Section 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, LP is recalling 106 convenience kits labeled for C-section procedures due to a potentially contaminated component.
What this FDA recall tells you, and what most readers miss
This notice was issued by FDA on September 8, 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 after determining they contain a potentially contaminated component that was recalled by its manufacturer.
Which Products Are Affected
The recall affects 106 kits distributed nationwide in the states of AL, CA, FL, IL, KS, LA, MA, MD, MO, MS, MT, NV, NY, OH, OK, SC, TX, and WI. Affected products include:
- C-SECTION, Medline Kit SKU DYNJ904612L, UDI/DI 10198459495625 (each) / 40198459495626 (case), Lot Numbers 26FMC710 and 26DMG417
- C-SECTION, Medline Kit SKU DYNJ911755, UDI/DI 10198459523946 (each) / 40198459523947 (case), Lot Number 25KMI628
- AHR C-SECTION KIT, Medline Kit SKU DYNJ912014, UDI/DI 10198459599569 (each) / 40198459599560 (case), Lot Numbers 26ABJ549, 26ABI899, and 25LBT433
This is FDA Class II recall number Z-3026-2026.
What You Should Do
Customers should contact Medline Industries, LP regarding the recalled kits.
Why This Matters
The recall involves medical procedure kits that may contain a contaminated component, representing a medium-risk situation under FDA Class II classification.
Source
FDA recall Z-3026-2026; 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 (1,202 characters here).
Similar severity timing
Same severity (medium) notices issued closest in time to September 8, 2026.
Frequently Asked Questions
Common questions about this FDA recall.