Recall of Centurion Medical Kits by Medline Industries
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 120 kits of Universal Central/Art Line Insertion Kit due to non-sterile alcohol prep pads containing a contaminant.
What this FDA recall tells you, and what most readers miss
This notice was issued by FDA on May 14, 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 is recalling specific items and lots of Medline Kits because they contain Webcol Large Alcohol Prep Pads that are non-sterile, following the discovery of a contaminant during a routine sterilization dose audit.
Which Products Are Affected
The affected products are Universal Central/Art Line Insertion Kit, Medline Kit SKU ART155A. The recall involves 120 kits with Lot Numbers: 2025100890 and 2026011290. UDI/DI codes are 10653160316459 for each and 00653160316452 for cases. Distribution is US Nationwide.
What You Should Do
Consumers should stop using the affected kits and contact Medline Industries, LP for instructions, as the firm has initiated notifications via methods such as email, fax, letter, press release, telephone, or visit.
Why This Matters
This recall highlights potential risks associated with non-sterile medical devices, affecting 120 kits distributed nationwide and emphasizing the need for proper sterilization in healthcare products.
Source
Recalled by FDA under recall number Z-2039-2026. For more information, refer to the FDA website.
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 (1,118 characters here).
Similar severity timing
Same severity (medium) notices issued closest in time to May 14, 2026.
Frequently Asked Questions
Common questions about this FDA recall.