Manufacturer

Argon Medical Devices, Inc

50 recalls in our database name Argon Medical Devices, Inc as the manufacturing or recalling firm.

What the numbers show

Total: 50
Critical: 0
Severe: 14
Most recent: 2026-08-05

Of the 50 recalls from Argon Medical Devices, Inc we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 14 (28%) are Severe.

About this listing

The manufacturer string comes from the agency’s own source notice — for FDA recalls, the “recalling firm” field; for NHTSA recalls, the vehicle manufacturer; for CPSC recalls, the firm-of-record on the joint press release. A single corporate family can appear under multiple manufacturer strings as agency notices aren’t standardized on a canonical name. If you don’t see recalls you expect, try a parent-company search or a broader full-text search.

Severity scores below are computed from the agency’s classification and the recall text, never from manufacturer behaviour or history. Many manufacturers issue routine corrective actions (software updates, labelling corrections) that are correctly scored low — having recalls on this list isn’t inherently a quality signal.

26–50 of 50

HighFDA (Devices)·Z-1937-2020·2020-05-20
Argon Medical Devices Recalls Arterial Line Kits Due to Needle Defect
Argon Medical Devices is recalling Arterial Line Kits because they contain a thicker suture and curved needle that may increase the risk of needle sticks.
Product
Arterial Line Kit 20ga X 3", Model 498106, Rx Only, Sterile EO, UDI: 00886333215577 - Product Usage: Arterial Catheters are indicated for use when in instances where continuous invasive blood pressure readings and/or frequent blood gas measurements are required. Case Label…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1936-2020·2020-05-20
Argon Medical Devices Recalls Arterial Line Kits Due to Needle Defect
Argon Medical Devices is recalling 150 Arterial Line Kits because they contain a thicker suture and curved needle that may increase the risk of needle sticks.
Product
Arterial Line Kit 20ga X 3", Model 498411B, Rx Only, Sterile EO, UDI: 00886333215652 - Product Usage: Arterial Catheters are indicated for use when in instances where continuous invasive blood pressure readings and/or frequent blood gas measurements are required. Case Label…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1791-2020·2020-05-13
Argon Medical Devices Recalls 0.035 Inch Guidewires Due to Tissue Perforation
Argon Medical Devices is recalling specific 0.035-inch guidewires because the stiffness of the soft end caused tissue perforation. The affected units were distributed to several countries outside the United States.
Product
0.035"(.89mm)x80 cm guidewire. Model 114135080. Soft Tip 3.5cm. REF/UDI: 114135080/(01)208863333008067. RxOnly STERILE EO
Category
Medical Device
Distribution
0 states
SevereFDA (Devices)·Z-1792-2020·2020-05-13
Argon Medical Devices Recalls 0.035 Inch Guidewires Due to Tissue Perforation Risk
Argon Medical Devices is recalling specific 0.035-inch guidewires because the soft tip stiffness caused tissue perforation. The affected units were distributed to several countries outside the US.
Product
0.035"(.89mm)x150 cm guidewire. Model 114135150. Soft Tip 3.5cm. REF/UDI: 114135150/(01)20886333008074. RxOnly.STERILE EO
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-0288-2020·2019-11-13
Argon Medical Devices Recalls Sterile Adapters Due to Seal Defects
Argon Medical Devices is recalling specific lots of sterile double female and male luer lock adapters because incomplete pouch seals may compromise sterility.
Product
(1) Argon Medical Devices Double Female LL Adapter, Special Adapter to Convert a Male Fitting to Female LL, REF 040183000A, 25/box, Sterile, Rx; and (2) Argon Medical Devices Double Male LL Adapter, Special Adapter to Convert a Female Fitting to Male LL, REF 040184000A…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0296-2020·2019-11-13
Argon Medical Devices Recalls AHD Luer Lock Caps Due to Seal Defect
Argon Medical Devices is recalling 49,130 AHD Luer Lock Caps because an incomplete seal may cause loss of sterility.
Product
Argon Medical Devices AHD Luer Lock Cap, REF 501303, Sterile, Rx. The firm name on the label is Argon Medical Devices, Inc., Athens, TX.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0290-2020·2019-11-13
Argon Medical Devices Recalls Stopcocks Due to Incomplete Pouch Seals
Argon Medical Devices is recalling specific stopcock products because incomplete pouch seals may cause a loss of sterility.
Product
(1) Argon Medical Devices Stopcocks, Clear 4-Way Stopcock w/Male Luer Lock, REF 041210002A, 25/box, Sterile, Rx; (2) Argon Medical Devices Stopcocks, 1-Way w/Male Luer Lock, REF 041216000A, 25/box, Sterile, Rx; (3) Argon Medical Devices Stopcocks, Double 4-Way Stopcock…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0291-2020·2019-11-13
Argon Medical Devices Recalls TRI-JECT IV Organizers Due to Seal Defect
Argon Medical Devices is recalling 49,130 units of TRI-JECT 3 Way IV Administration Organizers because an incomplete seal may cause loss of sterility.
Product
Argon Medical Devices TRI-JECT, 3 Way IV Administration Organizer without Stopcock, REF 041230001A, 25/box, Sterile, Rx. The firm name on the label is Argon Medical Devices, Inc., Athens, TX.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0292-2020·2019-11-13
Argon Medical Devices Recalls Luer Lock Plugs Due to Seal Defect
Argon Medical Devices is recalling specific lots of Luer Lock Plugs because an incomplete seal may cause a loss of sterility.
Product
Argon Medical Devices Plugs, Male/Female Luer Lock Plug, REF 041295000A, 50/box, Sterile, Rx. The firm name on the label is Argon Medical Devices, Inc., Athens, TX.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0295-2020·2019-11-13
Argon Medical Devices Septishield II Recalled for Potential Sterility Loss
Argon Medical Devices is recalling Septishield II products because an incomplete seal may cause a loss of sterility.
Product
Argon Medical Devices Septishield II, 80 cm, REF 497302, 25/box, Sterile, Rx. The firm name on the label is Argon Medical Devices, Inc., Athens, TX.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0294-2020·2019-11-13
Argon Medical Devices Hemostasis Valve Recall for Incomplete Pouch Seals
Argon Medical Devices is recalling Hemostasis Valves because incomplete pouch seals may cause a loss of sterility.
Product
Argon Medical Devices Hemostasis Valve, 7F-9F, REF 049297, Single Use Only, Non-Sterile-Further Processing Required, 250 valves/bag which is placed in a box. The firm name on the label is Argon Medical Devices, Inc., Athens, TX.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0293-2020·2019-11-13
Argon Medical Devices Recalls Vascuclamp Vascular Clamps Due to Sterility Risk
Argon Medical Devices is recalling Vascuclamp radiopaque vascular clamps because an incomplete pouch seal may cause a loss of sterility.
Product
(1) Argon Medical Devices Vascuclamp, Radiopaque Vascular Clamp, Small Straight, REF 046-1-200, 2 clamps/package, 5 packages/box, 10 boxes/case, Sterile, Rx; (2) Argon Medical Devices Vascuclamp, Radiopaque Vascular Clamp, Medium Straight, REF 046-1-300, 2 clamps per package…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0289-2020·2019-11-13
Argon Medical Devices Recalls Double Male LL Adapter Due to Seal Defect
Argon Medical Devices is recalling Double Male LL Adapters because an incomplete pouch seal may cause a loss of sterility.
Product
Argon Medical Devices Double Male LL Adapter, REF 040184800A, bulk, non-sterile. The firm name on the label is Argon Medical Devices, Inc., Athens, TX.
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-2252-2017·2017-06-14
Argon Medical Recalls Arterial Access Needles Due to Packaging Defect
Argon Medical Devices is recalling specific arterial access needles due to a potential packaging defect involving unsealed pouches.
Product
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/4; Clear Flashback Needle 7 cm x 19G AMC/4 Usage: Argon Arterial Access Needles are designed to provide vascular access for the percutaneous introduction…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1194-2017·2017-02-22
Argon Medical Devices Recalls Bone Marrow Aspiration Needles Due to Sterility Risk
Argon Medical Devices is recalling specific bone marrow aspiration needles because a potential defect in the blister packaging may compromise the sterility of the product.
Product
BONE MARROW ASPIRATION NEEDLE 15G x 2.688 MAX and 15G x 4 MAX Intended for the purpose of harvesting bone and/or bone marrow specimens
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1195-2017·2017-02-22
Argon Medical Devices Recalls T-LOK Bone Marrow Biopsy Needles
Argon Medical Devices is recalling T-LOK bone marrow biopsy needles due to a potential defect in the blister packaging that may compromise sterility.
Product
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 purpose of harvesting bone and/or bone marrow specimens
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1196-2017·2017-02-22
Argon Medical Devices Recalls Harvest Needles Due to Sterility Concerns
Argon Medical Devices is recalling 15 boxes of Harvest Needles because a potential defect in the blister packaging may compromise the sterility of the product.
Product
HARVEST NEEDLE 15GA X 2 Intended for the purpose of harvesting bone and/or bone marrow specimens
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0051-2017·2016-10-12
Argon Medical Devices Recalls MicroStic Plus Sheaths Due to Dilator Hub Defect
Argon Medical Devices is recalling 200 units of MicroStic Plus sheaths because the dilator hub is too small to secure the dilator to the sheath.
Product
MicroStic Plus w/SS Wire 5F and MicroStic Plus w/NiTi Wire & Echo Needle 4F. A sheath used to facilitate placing a catheter through the skin into a vein or artery.
Category
Medical Device
Distribution
2 states
HighFDA (Devices)·Z-1029-2016·2016-03-09
Argon Medical Devices Recalls ClosureFast Introducer Sheath Sets Due to Assembly Error
Argon Medical Devices is recalling specific ClosureFast Introducer Sheath Sets because incorrect sheath lengths were assembled to the devices.
Product
ClosureFast Micro Introducer Sheath Set 7Fr/Ch(2.3mm) x 7 cm REF MIS-F707 and ClosureFast Introducer Sheath Set 7Fr/Ch(2.3mm) x 11 cm REF IS-7F11. Indicated for use in arterial and venous procedures requiring percutaneous introduction of intravascular devices.
Category
Medical Device
Distribution
1 state
HighFDA (Devices)·Z-2188-2015·2015-07-29
Argon Medical Devices Recalls Bone Marrow Aspiration Needles Due to Sterility Risk
Argon Medical Devices is recalling specific bone marrow aspiration needles because a potential defect in the blister packaging may compromise the sterility of the product.
Product
Bone Marrow Aspiration Needle 15G x 2.688 MAX, Part Number DBMNI1501; Bone Marrow Aspiration Needle 15G x 4 MAX, Part Number DBMNI1504; Bone Marrow Aspiration Needle 16G x 2.688 MAX, Part Number DBMNI1601
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-2189-2015·2015-07-29
Argon Medical Devices Recalls T-Lok Bone Marrow Biopsy Needles
Argon Medical Devices is recalling specific T-Lok bone marrow biopsy needles due to a potential defect in the blister packaging that may compromise sterility.
Product
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, Part Number DBMNJ1104TL; Bone Marrow Biopsy Needle 13G x 4, Part Number DBMNJ1304
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-2698-2014·2014-10-01
Argon UltraStream Hemodialysis Catheter Recalled for Luer Cracking
Argon Medical Devices is recalling UltraStream Chronic Hemodialysis Catheters because cracks may develop on the red arterial luer during attachment or manipulation.
Product
UltraStream Peel Away Kit; Model Numbers 32401524 (24 cm), 32401528 (28cm), 32401532 (32 cm), and 32401536 (36 cm) and 32402540 (40 cm) The Rex Medical UltraStream Chronic Hemodialysis Catheter is a chronic hemodialysis catheter that can achieve high flow rates at low…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2697-2014·2014-10-01
Argon UltraStream Hemodialysis Catheter Recall Due to Luer Cracking
Argon Medical Devices is recalling UltraStream Chronic Hemodialysis Catheters because the red arterial luer may crack during attachment or manipulation.
Product
UltraStream Exchange Kit Model Numbers 32001524 (24 cm), 32001528 (28cm), 32001532 (32 cm), and 32001536 (36 cm) and 32002540 (40 cm). The Rex Medical UltraStream Chronic Hemodialysis Catheter is a chronic hemodialysis catheter that can achieve high flow rates at low arterial…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2696-2014·2014-10-01
Argon UltraStream Hemodialysis Catheters Recalled for Luer Cracking Risk
Argon Medical Devices is recalling UltraStream Chronic Hemodialysis Catheters because cracks may develop on the red arterial luer during use.
Product
UltraStream Chronic Hemodialysis Catheter Standard Kit; Model Number 32101524 (24 cm), 32101528 (28cm), 32101532 (32 cm), and 32101536 (36 cm) and 32102540 (40 cm). The Rex Medical UltraStream Chronic Hemodialysis Catheter is a chronic hemodialysis catheter that can achieve high…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1946-2012·2012-07-18
Argon Safedraw Venous Close Loop System Recalled for Pouch Seal Defect
Argon Medical Devices is recalling 10 Safedraw Venous Close Loop System blood sampling sets in Missouri due to a potential pouch seal defect that may compromise the sterile barrier.
Product
Safedraw Venous Close Loop System, Blood Sampling Set, packaged in a tyvek bag, Model/Part Number 688695, Argon Critical Care Systems, Singapore Pte. Ltd., 198 Yishun Avenue 7, Singapore 768028. The blood sampling set is intended to be used for closed-loop blood sampling from…
Category
Medical Device
Distribution
1 state