Fresh Recalls

Argon Medical Devices recalls

8 recent recalls on record for Argon Medical Devices in connected official government data as of September 7, 2026 at 6:00 AM UTC.

Models with recalls

Arterial Line Kit 20ga x 6 (1)Bone Marrow Tray (1)General Biospy Tray (1)L-Cath Midline S/L Catheter 20ga (3F) 1mm x 20cm (1)L-Cath PICC S/L Peripherally Inserted Central Catheter (1)One-Piece Introducer Tray (1)T-Lok Bone Marrow Tray (1)Transvenous Pacing Electrode Tray w/ Bipolar Balloon Pacing Electrode 5F (1)

All Argon Medical Devices recalls

FDA Class II · Medical device · August 5, 2026

L-Cath Midline S/L Catheter 20ga (3F) 1mm x 20cm recall — Argon Medical Devices, Inc

Catheters, indicated for short/long-term peripheral access to central venous system for the administration of fluids, medications, nutrients; and sampling, may experience leaking a…

Official ID Z-2804-2026 · Official record ↗

FDA Class II · Medical device · August 5, 2026

L-Cath PICC S/L Peripherally Inserted Central Catheter recall — Argon Medical Devices, Inc

Catheters, indicated for short/long-term peripheral access to central venous system for the administration of fluids, medications, nutrients; and sampling, may experience leaking a…

Official ID Z-2803-2026 · Official record ↗

FDA Class I · Medical device · July 22, 2026

Bone Marrow Tray recall — Argon Medical Devices, Inc

Kits containing Lidocaine HCL Injection USP 1% 10mg/mL 5mL ampules subject to another recall recalled due to not meeting release criteria for sterility.

Official ID Z-2709-2026 · Official record ↗

FDA Class I · Medical device · July 22, 2026

Arterial Line Kit 20ga x 6 recall — Argon Medical Devices, Inc

Kits containing Lidocaine HCL Injection USP 1% 10mg/mL 5mL ampules subject to another recall recalled due to not meeting release criteria for sterility.

Official ID Z-2708-2026 · Official record ↗

FDA Class I · Medical device · July 22, 2026

T-Lok Bone Marrow Tray recall — Argon Medical Devices, Inc

Kits containing Lidocaine HCL Injection USP 1% 10mg/mL 5mL ampules subject to another recall recalled due to not meeting release criteria for sterility.

Official ID Z-2707-2026 · Official record ↗

FDA Class I · Medical device · July 22, 2026

General Biospy Tray recall — Argon Medical Devices, Inc

Kits containing Lidocaine HCL Injection USP 1% 10mg/mL 5mL ampules subject to another recall recalled due to not meeting release criteria for sterility.

Official ID Z-2706-2026 · Official record ↗

FDA Class I · Medical device · July 22, 2026

One-Piece Introducer Tray recall — Argon Medical Devices, Inc

Kits containing Lidocaine HCL Injection USP 1% 10mg/mL 5mL ampules subject to another recall recalled due to not meeting release criteria for sterility.

Official ID Z-2705-2026 · Official record ↗

FDA Class I · Medical device · July 22, 2026

Transvenous Pacing Electrode Tray w/ Bipolar Balloon Pacing Electrode 5F recall — Argon Medical Devices, Inc

Kits containing Lidocaine HCL Injection USP 1% 10mg/mL 5mL ampules subject to another recall recalled due to not meeting release criteria for sterility.

Official ID Z-2704-2026 · Official record ↗

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Compiled from official public-domain government data. Last checked September 7, 2026 at 6:00 AM UTC.