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Argon Medical Devices recalls - full list & free alerts

9 official U.S. recalls involving Argon Medical Devices in the last 12 months, most recently on 2026-08-05.

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Full list (9)

Argon Medical Devices, Inc: L-Cath PICC S/L Peripherally Inserted Central Catheter: 26ga (1.9F) 0.60mm x 30cm, REF: 384539; 18ga (3.5F) 1.15mm x 60cm, REF: 384464; Basi
Medical DevicesFDA (device) · 2026-08-05 · Class II
Argon Medical Devices, Inc: L-Cath Midline S/L Catheter 20ga (3F) 1mm x 20cm, REF: 384620
Medical DevicesFDA (device) · 2026-08-05 · Class II
Argon Medical Devices, Inc: Transvenous Pacing Electrode Tray w/ Bipolar Balloon Pacing Electrode 5F, REF: 008416A, 008566A
Medical DevicesFDA (device) · 2026-07-22 · Class I
Argon Medical Devices, Inc: One-Piece Introducer Tray, REF: 497455, 497434 cardiovascular
Medical DevicesFDA (device) · 2026-07-22 · Class I
Argon Medical Devices, Inc: General Biospy Tray, REF: GUTS1000
Medical DevicesFDA (device) · 2026-07-22 · Class I
Argon Medical Devices, Inc: T-Lok Bone Marrow Tray, REF: BMT1104STL; BMET1104TL; BMT1104CATL
Medical DevicesFDA (device) · 2026-07-22 · Class I
Argon Medical Devices, Inc: Arterial Line Kit 20ga x 6, REF: 400115A
Medical DevicesFDA (device) · 2026-07-22 · Class I
Argon Medical Devices, Inc: Bone Marrow Tray, REF: CB0033TL; CB0355TLA
Medical DevicesFDA (device) · 2026-07-22 · Class I
Argon Medical Devices, Inc: Option"ELITE Vena Cava Filter System REF 352506070E UDI-DI code: 00886333217151 The Option"ELITE Filter is indicated for the prevention
Medical DevicesFDA (device) · 2025-12-03 · Class II