L-Cath Midline S/L Catheter 20ga (3F) 1mm x 20cm, REF:… recallZ-2804-2026 · Argon Medical Devices, Inc · initiated Jun 15, 2026
Open, Classified
Is my device affected?
- Compare the model, catalog and lot or serial numbers on your device or its packaging with the code information below. A recall usually covers only specific models or lots.
- If yours is listed, follow the instructions from Argon Medical Devices, Inc or your healthcare provider. The company's action is summarized under what the company is doing.
- Do not stop using a prescribed or implanted device on your own — talk to your healthcare provider first.
Where to find your model and lot numbers · What recall classes and statuses mean
Why it was recalled
Catheters, indicated for short/long-term peripheral access to central venous system for the administration of fluids, medications, nutrients; and sampling, may experience leaking and/or cracking at the hub, which may lead to replacement, inability to flush/aspirate catheter, catheter occlusion, therapy interruption, blood loss, tissue irritation, bloodstream infection.
FDA root cause category: Device Design
What the company is doing
On 6/15/2026, recall notices were emailed to customers who were asked to do the following: 1) Provide this recall notice to all people who need to be aware within your organization or to any organization where the potentially affected product has been transferred. 2) Segregate, quarantine, and return affected devices to recalling firm. 3) Complete and return the response form via email [email protected] For additional information on this letter, please email [email protected]
Recall details
- Recall number
- Z-2804-2026
- Status
- Open, Classified
- Initiated by the company
- Jun 15, 2026
- Posted by the FDA
- Jul 24, 2026
- Recalling firm
- Argon Medical Devices, Inc
- Quantity
- 20
- Product code
- LJS
- FDA submissions
- K230669
- Distribution
- US: 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. OUS: MYS, CAN, SAU
Product description
L-Cath Midline S/L Catheter 20ga (3F) 1mm x 20cm, REF: 384620
Code information (models, lots, serial numbers)
REF/UDI-DI/Lot(Expiration): 384620/00886333210008/11490543(7/28/2026)
Devices named in this recall
1 device in the FDA device registry whose identifier appears in the recall's code information.
- L-Cath™ Midline S/L Midline Catheter 384620Argon Medical Devices, Inc. · Catheter, Intravascular, Therapeutic, Long-Term Greater Than 30 Days1 recall1 report
Other products in the same recall event
The FDA groups related products into one recall event (event 99333).
- Z-2803-2026 · Open, ClassifiedL-Cath PICC S/L Peripherally Inserted Central Catheter: 26ga (1.9F) 0.60mm x 30cm, REF: 384539; 18ga (3.5F) 1.15mm x 60cm, REF: 384464; Basic Kit 28GA (1.2F) x 25cm 1 Lumen), REF: …
Sources and updates
- Recall record: FDA Medical Device Recalls, file dated Oct 16, 2026 · View the FDA recall notice ↗
- Devices: FDA GUDID, file dated Oct 13, 2026. Devices are linked when their identifier (with a valid check digit) appears in the recall's code information.
- Page last rebuilt: Oct 16, 2026. Text above is shown as published by the FDA.
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