FDA Medical devices recall ·
L-Cath Midline S/L Catheter 20ga (3F) 1mm x 20cm recall
- Recall number
- Z-2804-2026
- Date
- (initiated June 15, 2026)
- Company / brand
- Argon Medical Devices, Inc
1445 Flat Creek Rd, Athens, TX, United States - Category
- Medical devices › Class II
- Classification
- Class II
- Status
- Ongoing
- Units affected
- 20
- Initiated by
- Voluntary: Firm initiated
Read the official FDA notice ↗
Product
L-Cath Midline S/L Catheter 20ga (3F) 1mm x 20cm, REF: 384620
Why was it 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.
What should you do?
FDA enforcement reports do not list a consumer remedy. Check the product codes below against what you have; if it matches, stop using it and follow the instructions in the firm's or FDA's official notice, or contact the company. If you have health concerns, contact your healthcare provider.
Product codes & lot numbers
REF/UDI-DI/Lot(Expiration): 384620/00886333210008/11490543(7/28/2026)
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
States: Arkansas California Colorado Connecticut Florida Georgia Iowa Idaho Illinois Indiana Kansas Massachusetts Maryland Michigan Minnesota Missouri Mississippi North Carolina North Dakota New Jersey Nevada New York Oregon Tennessee Texas Utah Virginia Washington
What does Class II mean?
Class II means use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or the probability of serious harm is remote.
Source: FDA (medical devices), recall Z-2804-2026. Official notice. Republished from public data; RecallFlag is not affiliated with the FDA.