Argon Medical Devices, Inc recalls
Every recall we track for Argon Medical Devices, Inc — 38 in all, from 2018–2026 — plus the complaints and injury reports the public filed about them. 5 are rated “stop using now”.
Recalls per year, by danger level
Recalls from Argon Medical Devices, Inc peaked in 2020 (11); 38 since 2017. 13% rated “stop using now”.
All FDA recall records for Argon Medical Devices, Inc since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 0 | 0 | 0 | 0 |
| 2018 | 2 | 0 | 7 | 0 | 9 |
| 2019 | 1 | 1 | 1 | 0 | 3 |
| 2020 | 1 | 9 | 1 | 0 | 11 |
| 2021 | 0 | 2 | 0 | 0 | 2 |
| 2022 | 0 | 0 | 1 | 0 | 1 |
| 2023 | 1 | 0 | 0 | 0 | 1 |
| 2024 | 0 | 0 | 2 | 0 | 2 |
| 2025 | 0 | 1 | 0 | 0 | 1 |
| 2026 (to date) | 0 | 1 | 6 | 1 | 8 |
Most common reasons for Argon Medical Devices, Inc recalls
What to do if you have a recalled Argon Medical Devices, Inc product
- Match the model, catalog or lot number on your device to the recall.
- Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
- Report problems to FDA MedWatch.
All Argon Medical Devices, Inc recalls
16 shown- Use cautionMedical device
Argon Medical Devices, Inc recalls L-Cath PICC S/L Peripherally Inserted Central Catheter: 26ga (1.9F) 0.60mm x 30cm, REF: 384539; 18ga (3.5F) 1.15mm x
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 MedicalJun 15, 2026 - Lower riskMedical device
Argon Medical Devices, Inc recalls General Biospy Tray, REF: GUTS1000
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 DevicesJun 1, 2026 - Use cautionMedical device
Argon Medical Devices, Inc recalls Option"ELITE Vena Cava Filter System REF 352506070E UDI-DI code: 00886333217151 The Option"ELITE Filter is indicated
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 DevicesSep 12, 2025 - Lower riskMedical device
Argon Medical Devices, Inc recalls BioPince Ultra Full Core Biopsy Instrument: REF: REF: 360-1080-01, 360-1080-02, 360-1080-03, 360-1580-01, 360-1580-02,
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 MedicalJul 2, 2024 - Lower riskMedical device
Argon Medical Devices, Inc recalls L-CATH PICC S/L Peripherally Inserted Central Catheter, 26Ga (1.9F) 0.60mm x 30cm, REF: 384539
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 DevicesJun 14, 2024 - Stop using nowMedical device
Argon Medical Devices, Inc recalls Argon Medical Devices, REF 352506070E, Option Elite Retrievable Vena Cava Filter, Suitable of Jugular or Femoral
Argon Medical recalls Elite Retrievable Vena Cava Filters due to potential failure causing pulmonary embolism. Affected units have specific model and lot numbers.
Argon MedicalJun 8, 2023 - Lower riskMedical device
Argon Medical Devices, Inc recalls 1. Arterial Line Kit 20ga x 6" 2. Arterial Line Kit /1 20ga x 6"
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 DevicesJan 24, 2022 - Use cautionMedical device
Argon Medical Devices, Inc recalls SuperCore Biopsy Instrument: REF/Product Description: 701114090/SUPERCORE BIOPSY INSTR 14GA X 9CM; 701114150/SUPERCORE
Argon Medical Devices recalls SuperCore biopsy instruments with serial numbers listed. Component detachment could cause injury during medical procedures.
Argon Medical DevicesOct 4, 2021 - Use cautionMedical device
Argon Medical Devices, Inc recalls Scorpion Portal Vein Access Set - Product Usage: used to gain access to the hepatic vein and guide a sharp puncture
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 DevicesJul 8, 2021 - Use cautionMedical device
Argon Medical Devices, Inc recalls Argon Medical Devices TLAB, Transjugular Liver Biopsy System, REF: TL - 18C, 1/18 GA Flexcore Biopsy Needle, 1/7F
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 DevicesDec 10, 2020 - Lower riskMedical device
Argon Medical Devices, Inc recalls ClosureFast Micro Introducer Sheath Set, REF MIS-7F11; 7Fr/Ch (2.3mm)x11 cm. STERILE|EO; Rx ONLY - Product Usage:
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 DevicesJun 19, 2020 - Use cautionMedical device
Argon Medical Devices, Inc recalls Skater Introducer Set 6F x 18cm. REF/UDI: 651506300/(01)00886333005000; 655506300/(01)00886333005079 - Product Usage:
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 MedicalApr 26, 2020 - Use cautionMedical device
Argon Medical Devices, Inc recalls PAC Tray/5 Catheter Introducer Tray 8F, Model 497424, Rx Only, STERILE EO, UDI: 00886333214440 - Product Usage: The
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 MedicalApr 8, 2020 - Use cautionMedical device
Argon Medical Devices, Inc recalls 0.035"(.89mm)x150 cm guidewire. Model 114135150. Soft Tip 3.5cm. REF/UDI: 114135150/(01)20886333008074. RxOnly.STERILE
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 DevicesDec 4, 2019 - Lower riskMedical device
Argon Medical Devices, Inc recalls BioPince Full Core Biopsy Instrument 16ga x 15cm.,Use with Optional CO-Axial Needle MCXS1615BP. QTY.: 5/CS - Product
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 DevicesDec 2, 2019 - Lower riskMedical device
Argon Medical Devices, Inc recalls (1) Argon Medical Devices Vascuclamp, Radiopaque Vascular Clamp, Small Straight, REF 046-1-200, 2 clamps/package, 5
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.
Argon Medical DevicesOct 16, 2018
Argon Medical Devices, Inc recall questions
How many recalls has Argon Medical Devices, Inc had?
38 recalls from Argon Medical Devices, Inc are on record with U.S. safety agencies, from 2018–2026.
What is the most recent Argon Medical Devices, Inc recall?
Argon Medical Devices, Inc recalls L-Cath PICC S/L Peripherally Inserted Central Catheter: 26ga (1.9F) 0.60mm x 30cm, REF: 384539; 18ga (3.5F) 1.15mm x, dated Jun 15, 2026. Every Argon Medical Devices, Inc recall is listed on this page, newest first.
Why are Argon Medical Devices, Inc products recalled?
The most common reasons on record: The stiffness of the soft end of the guidewire caused tissue perforation. (2).
What should I do if I have a recalled Argon Medical Devices, Inc product?
Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.
How do I get alerts for new Argon Medical Devices, Inc recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.