Argon Medical L-Cath Midline Catheter Recall
Areazine synthesizes this FDA recall directly from FDA's official public data feed. See our methodology for full source attribution and refresh cadence.
Argon Medical Devices, Inc. is recalling 20 units of L-Cath Midline S/L Catheter due to potential leaking or cracking at the hub.
What this FDA recall tells you, and what most readers miss
This notice was issued by FDA on August 13, 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
Argon Medical Devices, Inc. initiated a voluntary recall of certain L-Cath Midline catheters after reports that the devices may experience leaking and/or cracking at the hub. This could lead to catheter replacement, inability to flush or aspirate, occlusion, therapy interruption, blood loss, tissue irritation, or bloodstream infection.
Which Products Are Affected
The recall involves L-Cath Midline S/L Catheter 20ga (3F) 1mm x 20cm, REF: 384620. A total of 20 units are affected, distributed under lot 11490543 (expiration 7/28/2026) with UDI-DI 00886333210008. Distribution occurred in US states AR, CA, CO, CT, FL, GA, IA, ID, IL, IN, KS, MA, MD, MI, MN, MO, MS, NC, ND, NJ, NV, NY, OR, TN, TX, UT, VA, WA and internationally in MYS, CAN, SAU. The recall number is Z-2804-2026.
What You Should Do
Healthcare facilities and providers in possession of the affected product should follow the firm's instructions provided in the initial notification letter regarding the recalled devices.
Why This Matters
The Class II recall addresses a defect that may cause therapy interruption or infection risks during use of the catheters for fluid, medication, or nutrient administration.
Source
FDA recall Z-2804-2026 (event ID 99333), Argon Medical Devices, Inc., Athens, TX.
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 (1,301 characters here).
Similar severity timing
Same severity (medium) notices issued closest in time to August 13, 2026.
Frequently Asked Questions
Common questions about this FDA recall.