Medline Major Basin Set 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 is recalling 113,843 convenience kits containing 10mL Polycarbonate Colored Syringes due to unapproved design changes.
What this FDA recall tells you, and what most readers miss
This notice was issued by FDA on August 5, 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 after identifying unapproved design changes to the products outside of the 510(k) cleared by the FDA. The products were not initially reported in RES 98601.
Which Products Are Affected Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes, specifically MAJOR BASIN SET DYNJ85723. The affected product has UDI-DI 10195327538491 and Lot 24ABO130. A total of 113,843 kits are involved. Distribution was nationwide across the United States including AL, AR, AZ, CA, CO, CT, FL, GA, IL, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NE, NJ, NM, NV, NY, OH, OK, OR, PA, RI, TN, TX, VA, WI, WY and the country of Barbados.
What You Should Do Consumers should follow instructions provided in the firm's notification letter regarding the recalled products.
Why This Matters The recall addresses regulatory compliance issues with medical devices distributed across the United States and Barbados.
Source FDA recall Z-2588-2026, https://www.fda.gov
Original source: FDA Official Notice ↗
Related FDA Recalls
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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 (1,046 characters here).
Similar severity timing
Same severity (medium) notices issued closest in time to August 5, 2026.
Frequently Asked Questions
Common questions about this FDA recall.