Argon Medical Devices, Inc recalls Option"ELITE Vena Cava Filter System REF 352506070E UDI-DI code: 00886333217151 The Option"ELITE Filter is indicated for the…
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 venous intimal injuries if excessive force is…
Read the official notice →- Date
- 2025-12-03
- Country
- United States
- Brand
- Argon Medical Devices
- Product
- Option"ELITE Vena Cava Filter System REF 352506070E UDI-DI code: 00886333217151 The Option"ELITE Filter is indicated for the prevention of…
- Classification
- Class II
- Units
- U.S. (nationwide) distribution to states of: AL, AR, AZ, CA, CO, CT, DC, FL,…
- Category
- Drugs & medical
- Source
- FDA · Device
Copied automatically from the US Food and Drug Administration. Details may be shortened or out of date; the official notice is the authoritative source. Disclaimer
What to do
- Check the product name, strength and lot number against the official notice.
- Do not stop a prescribed medicine without talking to your doctor or pharmacist first.
- Ask the pharmacy or supplier about a replacement or refund.
General guidance from Recall Atlas. The official notice from the US Food and Drug Administration has the exact models, batch codes and remedy, and it takes priority.
More Argon Medical Devices recalls
- 2026-08-05
USArgon Medical Devices, Inc recalls L-Cath Midline S/L Catheter 20ga (3F) 1mm x 20cm, REF: 384620
Catheters, indicated for short/long-term peripheral access to central venous system for the administration of fluids, medications, nutrients; and sampling, may experience leaking and/or cracking at the hub, which may…
FDA · DeviceArgon Medical Devices, IncUS: AR, CA, CO, CT, FL, GA, IA, ID, IL, IN, KS, MA, MD, MI, MN, MO, MS, NC,…Official notice →- 2026-07-22
- US
Argon Medical Devices, Inc recalls General Biospy Tray, REF: GUTS1000
Kits containing Lidocaine HCL Injection USP 1% 10mg/mL 5mL ampules subject to another recall recalled due to not meeting release criteria for sterility.
FDA · DeviceArgon Medical Devices, IncDistribution US nationwide including Puerto Rico; OUS to Trinidad and Tobago.Official notice → - 2024-10-02
- US
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, 360-1580-03,…
Holes have been identified in biopsy instrument packaging trays compromising the sterile barrier, which may lead to cross contamination, or the introduction of micro-organisms into the access site, which could lead to…
FDA · DeviceArgon Medical Devices, IncWorldwide - US Nationwide distribution including in the states of AZ, FL, OH,…Official notice → - 2024-08-21
- US
Argon Medical Devices, Inc recalls L-CATH PICC S/L Peripherally Inserted Central Catheter, 26Ga (1.9F) 0.60mm x 30cm, REF: 384539
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.
FDA · DeviceArgon Medical Devices, IncUS distribution to the states of: TX, WA, CA, ILOfficial notice → - 2023-08-02
- US
Argon Medical Devices, Inc recalls Argon Medical Devices, REF 352506070E, Option Elite Retrievable Vena Cava Filter, Suitable of Jugular or Femoral Delivery, STERILEO,…
There is the potential that the vena Cava Filter may not perform as intended which may result in pulmonary embolism.
FDA · DeviceArgon Medical Devices, IncUS Nationwide distribution in the state of TX.Official notice → - 2022-02-16
- US
Argon Medical Devices, Inc recalls 1. Arterial Line Kit 20ga x 6" 2. Arterial Line Kit /1 20ga x 6"
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 and minor blood loss.
FDA · DeviceArgon Medical Devices, IncUS Nationwide distribution in the states of AL, CA, DE, IL, IN, LA, MT, NV,…Official notice →
Other drugs & medical recalls in the United States
- 2025-12-03
- US
Noah Medical Corporation recalls Brand Name: Galaxy System Product Name: Galaxy System Model/Catalog Number: GAL-001 Product Description: The Galaxy SystemTM and its…
Due to Users not having access to the Instructions for Use/User Manual due to it being password protected.
FDA · DeviceNoah Medical CorporationUS distribution to states of: NY, MA, WV, WY, TN, OH, NJ, MN, CA, MO, ID, IN,…Official notice → - US
Inpeco S.A. recalls FlexLab (FLX); Version: FLX-217-40;
The Aliquoter Module (mALX) may generate secondary sample tubes without labels or with mismatched labels which may result in delayed results or erroneous results, this error occurs if the operators open the printer…
FDA · DeviceInpeco S.A.US Domestic: MI. OUS International: Australia, Finland, France, Germany,…Official notice → - US
Medtronic MiniMed, Inc. recalls CareLink Clinic, REF: MMT-7350
Software error causing incorrect data to be displayed on the 24-hour Sensor Glucose Overview Graph, any potential therapy decisions were made based on the incorrect data displayed on the 24-hour sensor glucose overview…
FDA · DeviceMedtronic MiniMed, Inc.Worldwide Distribution: US (nationwide) including states of: TX, NC, MN, CA,…Official notice → - US
Pivotal Health Solutions, Inc. recalls Quantum Intersegmental Table, Model/Catalog Number: Q400; heated massage table
The heat function may become damaged over time due to patients pressing on the areas with heat function components. Damage to components can lead to overheating which can lead to smoldering and melting of the vinyl…
FDA · DevicePivotal Health Solutions, Inc.Distribution to US nationwide, Canada and Japan.Official notice → - US
Remel, Inc recalls 1. CAMHB W/LHB, MANUAL, 11ML, 10/BOX YCP112-10 2. BRUCELLA BROTH, 11ML, 10/BOX YT3450
Products may contain contamination, which may result in a darker or brown media color.
FDA · DeviceRemel, IncWorldwide - US Nationwide distribution in the states of AK, CA, FL, GA, IA,…Official notice → - US
Magellan Diagnostics, Inc. recalls The LeadCare¿ II Blood Lead Test System relies on electrochemistry and a unique Sensor to detect lead in whole blood. The LeadCare¿ II…
Calibration Buttons being used in the kitting process were incorrectly labeled as Lot 2323M for lot 2333M. The use of mislabeled calibration Button with Lot #2333 can lead to delayed or erroneous high or erroneous low…