FDAFDA recall Z-2804-2026 · Aug 5, 2026
Argon Medical Devices, Inc: L-Cath Midline S/L Catheter 20ga (3F) 1mm x 20cm recall
Recall found
Product
L-Cath Midline S/L Catheter 20ga (3F) 1mm x 20cm, REF: 384620
Reason for recall
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.
What to do
FDA enforcement reports don't include consumer instructions. Check the codes below against your packaging. If this is a medicine or device you use, talk to your pharmacist or doctor before you stop or change anything, and contact the company or FDA for what to do with the product.
Recall details
- FDA classification
- Class II: use of or exposure to the product may cause temporary or medically reversible health problems, or the chance of serious problems is remote.
- Status
- Ongoing
- Codes, lots and dates
- REF/UDI-DI/Lot(Expiration): 384620/00886333210008/11490543(7/28/2026)
- Quantity
- 20
- 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
- Recalling firm
- Argon Medical Devices, Inc, Athens, TX
- Voluntary or mandated
- Voluntary: Firm initiated
- Recall started
- 2026-06-15
Source: openFDA enforcement record Z-2804-2026 · search recall number Z-2804-2026 in FDA's Enforcement Report.
Copied from the agency record without changes. Data as of Oct 22, 2026, 4:56 AM EDT. The agency notice is the final word.