Argon Medical Devices, Inc: 20 recalls on record

Recalls filed with 1 agency: FDA (20).

First recall on record: July 18, 2012. Most recent: August 5, 2026.

Risk classification: Class I: 6 · Class II: 14

Most recent recalls

DateAgencyProduct
August 5, 2026FDAL-Cath Midline S/L Catheter 20ga (3F) 1mm x 20cm, REF: 384620Z-2804-2026
August 5, 2026FDAL-Cath PICC S/L Peripherally Inserted Central Catheter: 26ga (1.9F) 0.60mm x 30cm, REF: 3…Z-2803-2026
July 22, 2026FDAArterial Line Kit 20ga x 6, REF: 400115AZ-2708-2026
July 22, 2026FDAT-Lok Bone Marrow Tray, REF: BMT1104STL; BMET1104TL; BMT1104CATLZ-2707-2026
July 22, 2026FDAGeneral Biospy Tray, REF: GUTS1000Z-2706-2026
July 22, 2026FDABone Marrow Tray, REF: CB0033TL; CB0355TLAZ-2709-2026
July 22, 2026FDATransvenous Pacing Electrode Tray w/ Bipolar Balloon Pacing Electrode 5F, REF: 008416A, 0…Z-2704-2026
July 22, 2026FDAOne-Piece Introducer Tray, REF: 497455, 497434 cardiovascularZ-2705-2026
October 2, 2024FDABioPince Ultra Full Core Biopsy Instrument: REF: REF: 360-1080-01, 360-1080-02, 360-1080-…Z-3192-2024
August 21, 2024FDAL-CATH PICC S/L Peripherally Inserted Central Catheter, 26Ga (1.9F) 0.60mm x 30cm, REF: 3…Z-2638-2024
February 16, 2022FDA1. Arterial Line Kit 20ga x 6" 2. Arterial Line Kit /1 20ga x 6"Z-0563-2022
September 29, 2021FDAScorpion Portal Vein Access Set - Product Usage: used to gain access to the hepatic vein …Z-2501-2021
November 13, 2019FDAArgon Medical Devices TRI-JECT, 3 Way IV Administration Organizer without Stopcock, REF 0…Z-0291-2020
November 13, 2019FDA(1) Argon Medical Devices Vascuclamp, Radiopaque Vascular Clamp, Small Straight, REF 046-…Z-0293-2020
February 22, 2017FDAT-LOK BONE MARROW BIOPSY NEEDLE 8G x 4 EXT CAN; T-LOK BONE MARROW BIOPSY NEEDLE 11G x 4 E…Z-1195-2017
February 22, 2017FDAHARVEST NEEDLE 15GA X 2 Intended for the purpose of harvesting bone and/or bone marrow…Z-1196-2017
October 1, 2014FDAUltraStream Chronic Hemodialysis Catheter Standard Kit; Model Number 32101524 (24 cm), 32…Z-2696-2014
October 1, 2014FDAUltraStream Exchange Kit Model Numbers 32001524 (24 cm), 32001528 (28cm), 32001532 (32 cm…Z-2697-2014
October 1, 2014FDAUltraStream Peel Away Kit; Model Numbers 32401524 (24 cm), 32401528 (28cm), 32401532 (32 …Z-2698-2014
July 18, 2012FDASafedraw Venous Close Loop System, Blood Sampling Set, packaged in a tyvek bag, Model/Par…Z-1946-2012

Questions about this company

How many recalls does Argon Medical Devices, Inc have?
Recalert has 20 U.S. recalls on record for Argon Medical Devices, Inc, published between July 18, 2012 and August 5, 2026.
What was the most recent Argon Medical Devices, Inc recall?
FDA recall Z-2804-2026, published August 5, 2026: L-Cath Midline S/L Catheter 20ga (3F) 1mm x 20cm, REF: 384620
Which agencies have handled Argon Medical Devices, Inc recalls?
Argon Medical Devices, Inc appears as the recalling firm in recalls from: FDA (20).

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