Argon Medical Devices, Inc

Frequent Recalls

8

Recalls

0

Units Recalled

0

Injuries

0

Deaths

Categories: Medical Device

2026-07-22 to 2026-08-05

Date	Source	Product	Brand	Severity	Units
2026-08-05	FDA Device	FDA Recall: L-Cath PICC S/L Peripherally Inserted Central Catheter: 26ga (1.9F) 0.60mm x 30cm, REF: 384539; 18ga	Argon Medical Devices, Inc	Class II	N/A
2026-08-05	FDA Device	FDA Recall: L-Cath Midline S/L Catheter 20ga (3F) 1mm x 20cm, REF: 384620	Argon Medical Devices, Inc	Class II	N/A
2026-07-22	FDA Device	FDA Recall: General Biospy Tray, REF: GUTS1000	Argon Medical Devices, Inc	Class I	N/A
2026-07-22	FDA Device	FDA Recall: Bone Marrow Tray, REF: CB0033TL; CB0355TLA	Argon Medical Devices, Inc	Class I	N/A
2026-07-22	FDA Device	FDA Recall: One-Piece Introducer Tray, REF: 497455, 497434 cardiovascular	Argon Medical Devices, Inc	Class I	N/A
2026-07-22	FDA Device	FDA Recall: T-Lok Bone Marrow Tray, REF: BMT1104STL; BMET1104TL; BMT1104CATL	Argon Medical Devices, Inc	Class I	N/A
2026-07-22	FDA Device	FDA Recall: Transvenous Pacing Electrode Tray w/ Bipolar Balloon Pacing Electrode 5F, REF: 008416A, 008566A	Argon Medical Devices, Inc	Class I	N/A
2026-07-22	FDA Device	FDA Recall: Arterial Line Kit 20ga x 6, REF: 400115A	Argon Medical Devices, Inc	Class I	N/A

Argon Medical Devices, Inc Recalls | WatchRecall