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Argon Medical Devices Recalls
50 recalls on record · July 18, 2012 to August 5, 2026 · Medical Devices
Recalls by year
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Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
November 13, 2019Medical DevicesFDA
Argon Medical Devices, Inc recalls Argon Medical Devices Septishield II, 80 cm, REF 497302, 25/box, Sterile, Rx. The firm name on the label is Argon Medic
Hazard: The seal formed on the edge of the pouch may be incomplete, which could result in a loss of sterility to the product.
November 13, 2019Medical DevicesFDA
Argon Medical Devices, Inc recalls Argon Medical Devices Hemostasis Valve, 7F-9F, REF 049297, Single Use Only, Non-Sterile-Further Processing Required, 250
Hazard: The seal formed on the edge of the pouch may be incomplete, which could result in a loss of sterility to the product.
November 13, 2019Medical DevicesFDA
Argon Medical Devices, Inc recalls (1) Argon Medical Devices Vascuclamp, Radiopaque Vascular Clamp, Small Straight, REF 046-1-200, 2 clamps/package, 5 pack
Hazard: The seal formed on the edge of the pouch may be incomplete, which could result in a loss of sterility to the product.
November 13, 2019Medical DevicesFDA
Argon Medical Devices, Inc recalls Argon Medical Devices Plugs, Male/Female Luer Lock Plug, REF 041295000A, 50/box, Sterile, Rx. The firm name on the labe
Hazard: The seal formed on the edge of the pouch may be incomplete, which could result in a loss of sterility to the product.
November 13, 2019Medical DevicesFDA
Argon Medical Devices, Inc recalls Argon Medical Devices TRI-JECT, 3 Way IV Administration Organizer without Stopcock, REF 041230001A, 25/box, Sterile, Rx.
Hazard: The seal formed on the edge of the pouch may be incomplete, which could result in a loss of sterility to the product.
November 13, 2019Medical DevicesFDA
Argon Medical Devices, Inc recalls (1) Argon Medical Devices Stopcocks, Clear 4-Way Stopcock w/Male Luer Lock, REF 041210002A, 25/box, Sterile, Rx; (2)
Hazard: The seal formed on the edge of the pouch may be incomplete, which could result in a loss of sterility to the product.
November 13, 2019Medical DevicesFDA
Argon Medical Devices, Inc recalls Argon Medical Devices Double Male LL Adapter, REF 040184800A, bulk, non-sterile. The firm name on the label is Argon Me
Hazard: The seal formed on the edge of the pouch may be incomplete, which could result in a loss of sterility to the product.
November 13, 2019Medical DevicesFDA
Argon Medical Devices, Inc recalls (1) Argon Medical Devices Double Female LL Adapter, Special Adapter to Convert a Male Fitting to Female LL, REF 04018300
Hazard: The seal formed on the edge of the pouch may be incomplete, which could result in a loss of sterility to the product.
June 14, 2017Medical DevicesFDA
Argon Medical Devices, Inc recalls Clear Flashback Needle 7cm x 18G AMC/4; Clear Flashback Needle 2.5 cm x 21G AMC/4; Winged Arterial Needle 7cm x 18G AMC/
Hazard: Argon Medical has received a complaint from one of their distributors of a potential packaging defect. The product is sealed in a pouch and the defect if present shows as a potential void or unsealed edge of the pouch.
February 22, 2017Medical DevicesFDA
Argon Medical Devices, Inc recalls HARVEST NEEDLE 15GA X 2 Intended for the purpose of harvesting bone and/or bone marrow specimens
Hazard: The recalling firm received a complaint from one of their customers of a potential defect in the forming of the primary package of the blister that may compromise the sterility of the product inside the tray.
February 22, 2017Medical DevicesFDA
Argon Medical Devices, Inc recalls T-LOK BONE MARROW BIOPSY NEEDLE 8G x 4 EXT CAN; T-LOK BONE MARROW BIOPSY NEEDLE 11G x 4 EXT CAN Intended for the purp
Hazard: The recalling firm received a complaint from one of their customers of a potential defect in the forming of the primary package of the blister that may compromise the sterility of the product inside the tray.
February 22, 2017Medical DevicesFDA
Argon Medical Devices, Inc recalls BONE MARROW ASPIRATION NEEDLE 15G x 2.688 MAX and 15G x 4 MAX Intended for the purpose of harvesting bone and/or bone
Hazard: The recalling firm received a complaint from one of their customers of a potential defect in the forming of the primary package of the blister that may compromise the sterility of the product inside the tray.
October 12, 2016Medical DevicesFDA
Argon Medical Devices, Inc recalls MicroStic Plus w/SS Wire 5F and MicroStic Plus w/NiTi Wire & Echo Needle 4F. A sheath used to facilitate placing a ca
Hazard: The supplier initiated a recall because affected lots of the micro-introducer have an outer diameter of the dilator hub that is slightly smaller than is capable of securing the dilator to the sheath
March 9, 2016Medical DevicesFDA
Argon Medical Devices, Inc recalls ClosureFast Micro Introducer Sheath Set 7Fr/Ch(2.3mm) x 7 cm REF MIS-F707 and ClosureFast Introducer Sheath Set 7Fr/Ch(2
Hazard: The incorrect sheath was assembled to the device so that the size 7 products received 11 cm sheaths and the size 11 product received 7 cm sheaths.
July 29, 2015Medical DevicesFDA
Argon Medical Devices, Inc recalls T-Lok Bone Marrow Biopsy Needle 8G x 4 Ext Can, Part Number DBMNJ0804TL; T-Lok Bone Marrow Biopsy Needle 11G x 4 Ext Can
Hazard: Potential defect in the forming of the primary package of the blister that may compromise the sterility of the product inside the tray.
July 29, 2015Medical DevicesFDA
Argon Medical Devices, Inc recalls Bone Marrow Aspiration Needle 15G x 2.688 MAX, Part Number DBMNI1501; Bone Marrow Aspiration Needle 15G x 4 MAX, Part Nu
Hazard: Potential defect in the forming of the primary package of the blister that may compromise the sterility of the product inside the tray.
October 1, 2014Medical DevicesFDA
Argon Medical Devices, Inc recalls UltraStream Peel Away Kit; Model Numbers 32401524 (24 cm), 32401528 (28cm), 32401532 (32 cm), and 32401536 (36 cm) and 3
Hazard: UltraStream Chronic Hemodialysis Catheter may develop cracks on the red (arterial) luer during attachment or manipulation.
October 1, 2014Medical DevicesFDA
Argon Medical Devices, Inc recalls UltraStream Exchange Kit Model Numbers 32001524 (24 cm), 32001528 (28cm), 32001532 (32 cm), and 32001536 (36 cm) and 320
Hazard: UltraStream Chronic Hemodialysis Catheter may develop cracks on the red (arterial) luer during attachment or manipulation.
October 1, 2014Medical DevicesFDA
Argon Medical Devices, Inc recalls UltraStream Chronic Hemodialysis Catheter Standard Kit; Model Number 32101524 (24 cm), 32101528 (28cm), 32101532 (32 cm)
Hazard: UltraStream Chronic Hemodialysis Catheter may develop cracks on the red (arterial) luer during attachment or manipulation.
July 18, 2012Medical DevicesFDA
Argon Medical Devices, Inc recalls Safedraw Venous Close Loop System, Blood Sampling Set, packaged in a tyvek bag, Model/Part Number 688695, Argon Critical
Hazard: Some of the kits may exhibit a potential defect with the pouch seal. The pouch issue may compromise the sterile barrier.