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

0Nov '24 0 0 0Feb 0 0 0May 0 0 0Aug 0 0 0Nov 1 0 0Feb 0 0 0May 0 6 2Aug 0 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: (1.9F) 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: (1.9F) 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	Sterility	Nationwide
21 Aug 2024Device	CLASS II	L-cath PICC S/L Peripherally Inserted Central Catheter (1.9F) recalled	Argon Medical Devices	Packaging Defects	4 states
2 Aug 2023Device	CLASS II	Argon Medical Devices, REF 352506070E, Option Elite Retrievable Vena recalled	Argon Medical Devices	Device Malfunction	Nationwide
16 Feb 2022Device	CLASS II	Arterial Line Kit Arterial Line Kit /1 recalled by Argon Medical Devices	Argon Medical Devices	Other	Nationwide
15 Dec 2021Device	CLASS II	701114090/supercore Biopsy Instr recalled by Argon Medical Devices	Argon Medical Devices	Other	Nationwide
29 Sep 2021Device	CLASS II	Scorpion Portal Vein Access Set recalled by Argon Medical Devices	Argon Medical Devices	Device Malfunction	Nationwide
17 Feb 2021Device	CLASS II	TLAB, Transjugular Liver Biopsy System recalled by Argon Medical Devices	Argon Medical Devices	Foreign Material	46 states
17 Feb 2021Device	CLASS II	TLAB, Transjugular Liver Biopsy System recalled by Argon Medical Devices	Argon Medical Devices	Foreign Material	46 states
17 Feb 2021Device	CLASS II	TLAB, Transjugular Liver Biopsy System recalled by Argon Medical Devices	Argon Medical Devices	Foreign Material	46 states
17 Feb 2021Device	CLASS II	TLAB, Transjugular Liver Biopsy System recalled by Argon Medical Devices	Argon Medical Devices	Foreign Material	46 states
17 Feb 2021Device	CLASS II	TLAB, Transjugular Liver Biopsy System recalled by Argon Medical Devices	Argon Medical Devices	Foreign Material	46 states
17 Feb 2021Device	CLASS II	TLAB, Transjugular Liver Biopsy System recalled by Argon Medical Devices	Argon Medical Devices	Foreign Material	46 states
26 Aug 2020Device	CLASS II	ClosureFast Micro Introducer Sheath Set recalled	Argon Medical Devices	Sterility	Nationwide
1 Jul 2020Device	CLASS II	BioPince Full Core Biopsy Instrument.,Use recalled	Argon Medical Devices	Packaging Defects	Nationwide
3 Jun 2020Device	CLASS II	Skater Introducer Set 6F recalled by Argon Medical Devices	Argon Medical Devices	Other	TX
20 May 2020Device	CLASS II	Arterial Line Kit recalled by Argon Medical Devices	Argon Medical Devices	Other	Nationwide
20 May 2020Device	CLASS II	Arterial Line Kit recalled by Argon Medical Devices	Argon Medical Devices	Other	Nationwide
20 May 2020Device	CLASS II	PAC Tray/5 Catheter Introducer Tray 8F recalled by Argon Medical Devices	Argon Medical Devices	Other	Nationwide
13 May 2020Device	CLASS I	0.035"(.89mm)x80 cm guidewire. Model 114135080. Soft Tip 3.5cm. recalled	Argon Medical Devices	Other	TX
13 May 2020Device	CLASS I	0.035"(.89mm)x150 cm guidewire. Model 114135150. Soft Tip 3.5cm. recalled	Argon Medical Devices	Other	TX
13 Nov 2019Device	CLASS II	Argon Medical Devices Stopcocks recalled	Argon Medical Devices	Sterility	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.