Every recall we track for Argon Medical Devices, Inc — 38 in all — plus the complaints and injury reports the public filed about them.
Argon Medical recalls specific PICC catheter models due to potential leaking or cracking at the hub, which may cause blood loss, infection, or therapy interruption. Affected units include 26ga and 18ga sizes with certain reference numbers.
Argon Medical Devices recalls L-Cath Midline S/L Catheter 20ga (3F) 1mm x 20cm (REF 384620) due to hub leaks and cracks causing infection risks. Affected patients should contact for remedy.
Argon Medical Devices recalls bone marrow trays with specific serial numbers due to potential sterility issues in lidocaine injections. Affected units may not meet safety standards for medical use.
Argon Medical Devices recalls T-Lok Bone Marrow Trays with specific serial numbers due to potential sterility issues. Affected units may not meet safety standards for medical use.
Argon Medical Devices recalls specific One-Piece Introducer Trays (REF: 497455, 497434) due to potential sterility issues in lidocaine kits. Affected units have unique serial numbers and expiration dates.
Argon Medical Devices recalls specific Transvenous Pacing Electrode Tray models due to potential sterility issues in lidocaine injection kits. Affected units may not meet safety standards for medical use.
Argon Medical recalls Arterial Line Kit 20ga x 6 (REF 400115A) due to potential sterility issues. Affected units have specific lot numbers expiring July 2027. Consumers should contact the company for details.
Argon Medical Devices recalls General Biospy Tray REF GUTS1000 due to potential sterility issues in lidocaine kits. Affected units have specific lot numbers and expiration dates.
Argon Medical Devices recalls Option ELITE Vena Cava Filter System REF 352506070E with UDI-DI code 00886333217151 due to potential venous intimal injuries from excessive force during procedure. Affected units include specific lot numbers.
Argon Medical recalls BioPince Ultra Full Core Biopsy Instruments with packaging holes that may cause infections. Affected models include 360-1080-01 to 370-1580-03 and specific lot numbers. Stop using if you have these items.
Argon Medical Devices recalls 26G PICC catheters labeled 30cm but containing 50cm length, potentially causing procedural delays. Affected units have specific lot and expiration dates.
Argon Medical recalls Elite Retrievable Vena Cava Filters due to potential failure causing pulmonary embolism. Affected units have specific model and lot numbers.
Argon Medical Devices recalls two lots of arterial line kits where the guidewire might not fit through the needle, potentially causing minor delays and blood loss during procedures.
Argon Medical Devices recalls SuperCore biopsy instruments with serial numbers listed. Component detachment could cause injury during medical procedures.
Argon Medical recalls Scorpion Portal Vein Access Sets with sheaths that crack at tips, posing a risk of injury during liver vein procedures. Affected items include specific stylets and needles sold with lot number 11369609.
Argon Medical Devices recalls TLAB liver biopsy kits with potential sheath separation during use, risking surgery. Affected units include specific lot numbers and models.
Argon Medical Devices recalls specific liver biopsy kits due to potential sheath separation during use, risking surgical intervention. Affected units include certain lot numbers of the TLAB system.
Argon Medical Devices recalls specific liver biopsy kits due to risk of sheath separation during use, potentially requiring surgery to prevent permanent damage.
Argon Medical Devices recalls TLAB liver biopsy kits with potential sheath separation causing surgical intervention. Affected models include TL-19 with specific lot numbers. Contact for remedy details.
Argon Medical Devices recalls TLAB liver biopsy kits with potential sheath separation during use, risking surgical intervention. Affected models include TL-19S with specific lot numbers.
Argon Medical Devices recalls TLAB liver biopsy kits with potential sheath separation during use, risking surgical intervention. Affected kits have specific lot numbers.
Argon Medical Devices recalls ClosureFast Micro Introducer Sheath Set (REF MIS-7F1: 7Fr/Ch 2.3mm x11 cm) due to sterile sheaths with different expiration dates. This affects medical devices used in vein/artery procedures.
Argon Medical recalls Skater Introducer Set 6F x 18cm due to risk of tungsten coils detaching from guidewires during use in non-vascular procedures.
Argon Medical recalls Arterial Line Kit 20ga X 3" Model 498411B due to curved needle requiring needle driver, risking needle sticks during surgery. Affected users should contact for remedy.
Argon Medical recalls Arterial Line Kit 20ga X 3" Model 498106 due to curved needle requiring needle driver, risking needle sticks during surgery. Affected users should contact for details.
Argon Medical recalls PAC Tray/5 Catheter Introducer Tray 8F Model 497424 due to curved needle requiring needle driver, risking needle sticks during surgery.
Argon Medical Devices recalls specific guidewire models due to soft tip stiffness causing tissue perforation. Affected units include model 114135080 with lot numbers 11235895, 11234476, 11237014, and 11240602. Contact for remedy details.
Argon Medical Devices recalls specific soft tip guidewires (Model 114135150) that may cause tissue perforation. Affected units include certain lot numbers from 2020-2021. Consumers should contact the company for details.
Argon Medical Devices recalls BioPince Full Core Biopsy Instruments due to incorrect labeling. This may cause confusion in medical use. Consumers should contact the manufacturer for details.
Argon Medical Devices recalls specific stopcock models due to potential incomplete seal causing loss of sterility. Affected products include 6 types with lot numbers; users should check their product details.
Argon Medical Devices recalls sterile Luer Lock Plugs due to potential incomplete seal causing sterility loss. Affected units include specific lot numbers from 2022. Consumers should contact the company for details.
Argon Medical Devices recalls Septishield II 80cm pouches (REF 497302) due to potential incomplete seals causing sterility loss. Affected units sold with lot numbers 11228251 and 11229805.
Argon Medical Devices recalls 250 single-use hemostasis valves (7F-9F) due to potential sterility loss from incomplete pouch seals. Affected units sold with lot number 11232311.
Argon Medical Devices recalls sterile AHD Luer Lock Caps (REF 501303) due to potential incomplete pouch seals risking product sterility. Affected lots 11228902 and 1123044: stop using immediately.
Argon Medical Devices recalls bulk non-sterile Double Male LL Adapters with incomplete pouch seals that could compromise sterility. Affected units have lot number 11229386. Consumers should contact the company for details.
Argon Medical Devices recalls double female and male LL adapters due to incomplete seal risking product sterility. Affected units have specific lot numbers and are sold sterile. Consumers should contact the company for details.
Argon Medical Devices recalls its TRI-JECT 3-way IV organizer (REF 041230001A) due to potential incomplete pouch seals causing sterility loss. Affected units sold in 2023-2024.
Argon Medical Devices recalls specific sterile surgical clamps due to potential incomplete pouch seals, risking loss of sterility during procedures. Affected models include Small Straight, Medium Straight, Medium Angled, and Large Angled clamps with certain lot numbers.
