Angiodynamics, Inc. recalls

All Angiodynamics, Inc. recalls we track from FDA, CPSC and NHTSA data. Categories: medical devices (22).

22 recalls published between January 8, 2025 and April 29, 2026. Most common issues: mislabeling (1).

• AccuVu Angiographic Catheter, Pigtail, Non-Braided, With 21 R/O Markers recall
  FDA April 29, 2026 · Angiodynamics, Inc. · Class II
• AccuVu Angiographic Catheter, Omni Flush, Non-Braided, With 21 R/O Markers recall
  FDA April 29, 2026 · Angiodynamics, Inc. · Class II
• AccuVu Angiographic Catheter, Straight Flush, Non-Braided… recall
  FDA April 29, 2026 · Angiodynamics, Inc. · Class II
• AccuVu Angiographic Catheter, Omni Flush, Non-Braided, With 2 R/O Markers recall
  FDA April 29, 2026 · Angiodynamics, Inc. · Class II
• Soft-Vu Angiographic Catheter, Kumpe, Non-Braided recall
  FDA April 29, 2026 · Angiodynamics, Inc. · Class II
• Soft-Vu Angiographic Catheter, Omni Flush, Non-Braided recall
  FDA April 29, 2026 · Angiodynamics, Inc. · Class II
• Soft-Vu Angiographic Catheter, Straight Art, Non-Braided recall
  FDA April 29, 2026 · Angiodynamics, Inc. · Class II
• Soft-Vu Angiographic Catheter, Headhunter (1), Non-Braided recall
  FDA April 29, 2026 · Angiodynamics, Inc. · Class II
• Soft-Vu Angiographic Catheter, Sos Omni Selective (1), Non-Braided recall
  FDA April 29, 2026 · Angiodynamics, Inc. · Class II
• Soft-Vu Angiographic Catheter, Kumpe, Non-Braided recall
  FDA April 29, 2026 · Angiodynamics, Inc. · Class II
• Soft-Vu Angiographic Catheter, Cobra (2), Non-Braided recall
  FDA April 29, 2026 · Angiodynamics, Inc. · Class II
• Soft-Vu Angiographic Catheter, Cobra (1), Non-Braided recall
  FDA April 29, 2026 · Angiodynamics, Inc. · Class II
• Soft-Vu Angiographic Catheter, Berenstein, Non-Braided recall
  FDA April 29, 2026 · Angiodynamics, Inc. · Class II
• Soft-Vu Angiographic Catheter, Kumpe, Non-Braided recall
  FDA April 29, 2026 · Angiodynamics, Inc. · Class II
• Soft-Vu Angiographic Catheter, Cobra (2), Non-Braided recall
  FDA April 29, 2026 · Angiodynamics, Inc. · Class II
• Soft-Vu Angiographic Catheter, Berenstein, Non-Braided recall
  FDA April 29, 2026 · Angiodynamics, Inc. · Class II
• Soft-Vu Angiographic Catheter, Pigtail, Non-Braided recall
  FDA April 29, 2026 · Angiodynamics, Inc. · Class II
• Soft-Vu Angiographic Catheter, Omni Flush, Non-Braided recall
  FDA April 29, 2026 · Angiodynamics, Inc. · Class II
• Soft -Vu Angiographic Catheter, Kumpe, Non-Braided recall
  FDA April 29, 2026 · Angiodynamics, Inc. · Class II
• Soft-Vu Angiographic Catheter, Pigtail, Non-Braided recall
  FDA April 29, 2026 · Angiodynamics, Inc. · Class II
• IsoLoc Short Profile Prostate Immobilization Treatment Balloon Device Kit recall
  FDA March 26, 2025 · Angiodynamics, Inc. · Class II
• AURYON LASER SYSTEM 100-120 VAC. Model Number: EXM001… recall
  FDA January 8, 2025 · Angiodynamics, Inc. · Class II