- Recalling firm
- Argon Medical Devices, Inc
- 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.
- Affected products (lot / model / serial)
- REF/UDI-DI/Lot(Expiration): 384620/00886333210008/11490543(7/28/2026)
- Units affected
- 20
- Distribution pattern
- 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
- Firm location
- Athens, TX, United States
- Recall type
- Voluntary: Firm initiated
- How the firm notified customers
- Letter
- Product type
- Devices
- Status
- Ongoing
- Recall number
- Z-2804-2026
- Recall initiated
- June 15, 2026
- FDA classification date
- July 24, 2026
- FDA report date
- August 5, 2026
- FDA event ID
- 99333
- Last updated on HTM Vibe
- August 11, 2026