Argon Medical Devices, Inc recalls
23 recalls in our records from 2012 to 2026: 23 FDA medical devices.
Recalls with full detail pages
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Argon Medical Devices, Inc medical device recall: Transvenous Pacing Electrode Tray w/ Bipolar Balloon Pacing Electrode…
Kits containing Lidocaine HCL Injection USP 1% 10mg/mL 5mL ampules subject to another recall recalled due to not meeting release criteria for sterility.
Earlier and other recalls
These link to the official agency notice.
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Argon Medical Devices, Inc medical device recall: L-Cath PICC S/L Peripherally Inserted Central Catheter: 26ga Official notice ↗
Catheters, indicated for short/long-term peripheral access to central venous system for the administration of fluids, medications, nutrients; and sampling, may…
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Argon Medical Devices, Inc medical device recall: Option"ELITE Vena Cava Filter System REF 352506070E UDI-DI code:… Official notice ↗
Due to complaints of increased resistance when advancing the dilator within the introducer sheath. This issue could potential result in procedural delays and/or risk of…
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Argon Medical Devices, Inc medical device recall: BioPince Ultra Full Core Biopsy Instrument: REF: REF: 360-1080-01 Official notice ↗
Holes have been identified in biopsy instrument packaging trays compromising the sterile barrier, which may lead to cross contamination, or the introduction of…
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Argon Medical Devices, Inc medical device recall: L-CATH PICC S/L Peripherally Inserted Central Catheter Official notice ↗
Peripherally Inserted Central Catheter (PICC) is labeled 26G/1.9Fr x 30cm but package contains incorrect 26G/1.9Fr x 50cm PICC, which could lead to procedural delay.
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Argon Medical Devices, Inc medical device recall: Argon Medical Devices Official notice ↗
There is the potential that the vena Cava Filter may not perform as intended which may result in pulmonary embolism.
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Argon Medical Devices, Inc medical device recall: 1. Arterial Line Kit 20ga x 6" 2. Arterial Line Kit /1 20ga x 6 Official notice ↗
Guidewire included with two lots of Arterial Line Kits would not fit through the needle of the same kit. This could potentially lead to a slight delay in the procedure…
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Argon Medical Devices, Inc medical device recall: SuperCore Biopsy Instrument: REF/Product Description:… Official notice ↗
Due to component (housing and plunger) detaching from the semi-automatic biopsy instruments.
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Argon Medical Devices, Inc medical device recall: Scorpion Portal Vein Access Set - Product Usage: used to gain access… Official notice ↗
As a result of design changes, sheaths have exhibited cracking/breaking at the tips.
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Argon Medical Devices, Inc medical device recall: Argon Medical Devices TLAB Official notice ↗
Due to a manufacturing error their is a potential that the sheath within the biopsy kit can separate during use if the tip is flexed or experiences bending stresses.…
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Argon Medical Devices, Inc medical device recall: ClosureFast Micro Introducer Sheath Set Official notice ↗
Sterile introducer sheath set manufactured under one lot with different expiration dates.
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Argon Medical Devices, Inc medical device recall: BioPince Full Core Biopsy Instrument 16ga x 15cm Official notice ↗
Incorrect product labeling.
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Argon Medical Devices, Inc medical device recall: Skater Introducer Set 6F x 18cm. REF/UDI: 651506300/(01)00886333005000 Official notice ↗
Tungsten coils of the guidewire included in the introducer kit were detaching.
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Argon Medical Devices, Inc medical device recall: Arterial Line Kit 20ga X 3 Official notice ↗
Arterial Line Kits include thicker curved reverse-cutting needle with a 0-silk suture, instead of the usual straight-cutting needle with a 3-0 silk suture. The thicker…
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Argon Medical Devices, Inc medical device recall: 0.035"(.89mm)x80 cm guidewire. Model 114135080. Soft Tip 3.5cm.… Official notice ↗
The stiffness of the soft end of the guidewire caused tissue perforation.
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Argon Medical Devices, Inc medical device recall: (1) Argon Medical Devices Double Female LL Adapter Official notice ↗
The seal formed on the edge of the pouch may be incomplete, which could result in a loss of sterility to the product.
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Argon Medical Devices, Inc medical device recall: Clear Flashback Needle 7cm x 18G AMC/4 Official notice ↗
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…
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Argon Medical Devices, Inc medical device recall: BONE MARROW ASPIRATION NEEDLE 15G x 2.688 MAX and 15G x 4 MAX… Official notice ↗
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…
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Argon Medical Devices, Inc medical device recall: MicroStic Plus w/SS Wire 5F and MicroStic Plus w/NiTi Wire & Echo… Official notice ↗
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…
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Argon Medical Devices, Inc medical device recall: ClosureFast Micro Introducer Sheath Set 7Fr/Ch(2.3mm) x 7 cm REF… Official notice ↗
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.
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Argon Medical Devices, Inc medical device recall: Bone Marrow Aspiration Needle 15G x 2.688 MAX Official notice ↗
Potential defect in the forming of the primary package of the blister that may compromise the sterility of the product inside the tray.
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Argon Medical Devices, Inc medical device recall: UltraStream Chronic Hemodialysis Catheter Standard Kit Official notice ↗
UltraStream Chronic Hemodialysis Catheter may develop cracks on the red (arterial) luer during attachment or manipulation.
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Argon Medical Devices, Inc medical device recall: Safedraw Venous Close Loop System Official notice ↗
Some of the kits may exhibit a potential defect with the pouch seal. The pouch issue may compromise the sterile barrier.
Firm names are matched across agencies by name only. Different companies with similar names may be grouped together; check each official notice.