Argon Medical Devices, Inc recalls

All Argon Medical Devices, Inc recalls we track from FDA, CPSC and NHTSA data. Categories: medical devices (9).

9 recalls published between December 3, 2025 and August 5, 2026. Most common issues: sterility (6), injury risk (1). 6 were FDA Class I, the most serious level.

• L-Cath Midline S/L Catheter 20ga (3F) 1mm x 20cm recall
  FDA August 5, 2026 · Argon Medical Devices, Inc · Class II
• L-Cath PICC S/L Peripherally Inserted Central Catheter: 26ga (1.9F) 0.60mm… recall
  FDA August 5, 2026 · Argon Medical Devices, Inc · Class II
• Bone Marrow Tray recall
  FDA July 22, 2026 · Argon Medical Devices, Inc · Class I
• Arterial Line Kit 20ga x 6 recall
  FDA July 22, 2026 · Argon Medical Devices, Inc · Class I
• T-Lok Bone Marrow Tray recall
  FDA July 22, 2026 · Argon Medical Devices, Inc · Class I
• General Biospy Tray recall
  FDA July 22, 2026 · Argon Medical Devices, Inc · Class I
• One-Piece Introducer Tray recall
  FDA July 22, 2026 · Argon Medical Devices, Inc · Class I
• Transvenous Pacing Electrode Tray w/ Bipolar Balloon Pacing Electrode 5F recall
  FDA July 22, 2026 · Argon Medical Devices, Inc · Class I
• Option"ELITE Vena Cava Filter System recall
  FDA December 3, 2025 · Argon Medical Devices, Inc · Class II