Argon Medical Devices, Inc: Catheter, Intravascular, Therapeutic, Long-term Greater Than 30 Days
Recall Summary Argon Medical Devices is recalling L-Cath Midline S/L Catheters (20ga, 3F, 1mm x 20cm) because the hub may leak or crack, potentially causing the catheter to stop working, become blocked, or allow blood to escape. These catheters are used to deliver medications, fluids, and nutrients to patients. The recall affects units distributed across most U.S. states, as well as Canada, Malaysia, and Saudi Arabia.
- Recalling firm
- Argon Medical Devices, Inc
- Product
- L-Cath Midline S/L Catheter 20ga (3F) 1mm x 20cm, REF: 384620
- Reason
- 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.
- Classification
- Class II
- Category
- medical device recall
- Country
- United States
- Agency
- FDA-DEVICES
- Recall date
- 2026-06-15
- Status
- Open, Classified
- Areas affected
- AR, CA, CO, CT, FL, GA, ID, IL, IN, IA, KS, MD, ...
- 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
Official recall notice from FDA-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/5bf92ce3-d381-4199-b5d7-dd61d2cfa1d5