Argon Medical Devices recalls

Argon Medical Devices has 50 recalls on record with the FDA and USDA, the earliest in 2012 and the latest reported on 5 Aug 2026. 15 are still ongoing. 9 were reported in the last 12 months. The most frequent reason is sterility.

Total recalls50since 2012

Last 12 months9reported

Class I816% of total

Ongoing15latest 5 Aug 2026

Recalls per month, last 24 months

click a bar for that month

1Oct '24 0 0 0Jan '25 0 0 0Apr 0 0 0Jul 0 0 0Oct 0 1 0Jan '26 0 0 0Apr 0 0 6Jul 2 0

Severity split

Class I 8 16%Class II 42 84%Class III 0 0%

Why argon medical devices is recalled

Product types

By year

2026816%
202512%
202424%
202312%
202212%
2021816%
2020816%
2019918%
201748%
201624%

Ongoing argon medical devices recalls

15 active

Reported	Class	Recall	Company	Reason	Where
5 Aug 2026Device	CLASS II	L-Cath PICC S/L Peripherally Inserted Central Catheter: 9F) recalled	Argon Medical Devices	Labeling Errors	28 states
5 Aug 2026Device	CLASS II	L-Cath Midline S/L Catheter (3F) recalled by Argon Medical Devices	Argon Medical Devices	Labeling Errors	28 states
22 Jul 2026Device	CLASS I	Bone Marrow Tray recalled by Argon Medical Devices	Argon Medical Devices	Sterility	Nationwide
22 Jul 2026Device	CLASS I	T-Lok Bone Marrow Tray recalled by Argon Medical Devices	Argon Medical Devices	Sterility	Nationwide
22 Jul 2026Device	CLASS I	One-Piece Introducer Tray recalled by Argon Medical Devices	Argon Medical Devices	Sterility	Nationwide
22 Jul 2026Device	CLASS I	Transvenous Pacing Electrode Tray w/ Bipolar Balloon Pacing recalled	Argon Medical Devices	Sterility	Nationwide

All argon medical devices recalls, newest first

50 total

Reported	Class	Recall	Company	Reason	Where
5 Aug 2026Device	CLASS II	L-Cath PICC S/L Peripherally Inserted Central Catheter: 9F) recalled	Argon Medical Devices	Labeling Errors	28 states
5 Aug 2026Device	CLASS II	L-Cath Midline S/L Catheter (3F) recalled by Argon Medical Devices	Argon Medical Devices	Labeling Errors	28 states
22 Jul 2026Device	CLASS I	Bone Marrow Tray recalled by Argon Medical Devices	Argon Medical Devices	Sterility	Nationwide
22 Jul 2026Device	CLASS I	T-Lok Bone Marrow Tray recalled by Argon Medical Devices	Argon Medical Devices	Sterility	Nationwide
22 Jul 2026Device	CLASS I	One-Piece Introducer Tray recalled by Argon Medical Devices	Argon Medical Devices	Sterility	Nationwide
22 Jul 2026Device	CLASS I	Transvenous Pacing Electrode Tray w/ Bipolar Balloon Pacing recalled	Argon Medical Devices	Sterility	Nationwide
22 Jul 2026Device	CLASS I	Arterial Line Kit recalled by Argon Medical Devices	Argon Medical Devices	Sterility	Nationwide
22 Jul 2026Device	CLASS I	General Biospy Tray recalled by Argon Medical Devices	Argon Medical Devices	Sterility	Nationwide
3 Dec 2025Device	CLASS II	Option"Elite Vena Cava Filter System recalled by Argon Medical Devices	Argon Medical Devices	Device Malfunction	Nationwide
2 Oct 2024Device	CLASS II	BioPince Ultra Full Core Biopsy Instrument recalled	Argon Medical Devices	Lead & Heavy Metals	Nationwide

About this list

Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.