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.
Read the official notice →- Date
- 2023-08-02
- Country
- United States
- Brand
- Argon Medical Devices
- Product
- Argon Medical Devices, REF 352506070E, Option Elite Retrievable Vena Cava Filter, Suitable of Jugular or Femoral Delivery, STERILEO,…
- Classification
- Class II
- Units
- US Nationwide distribution in the state of TX.
- 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 Details may be shortened or out of date; the official notice is the authoritative source.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
- 2026-07-22
USArgon 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 →- 2025-12-03
- US
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…
FDA · DeviceArgon Medical Devices, IncU.S. (nationwide) distribution to states of: AL, AR, AZ, CA, CO, CT, DC, FL,…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 → - 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 → - 2021-12-15
- US
Argon Medical Devices, Inc recalls SuperCore Biopsy Instrument: REF/Product Description: 701114090/SUPERCORE BIOPSY INSTR 14GA X 9CM; 701114150/SUPERCORE BIOPSY INSTR…
Due to component (housing and plunger) detaching from the semi-automatic biopsy instruments.
FDA · DeviceArgon Medical Devices, IncWorldwide distribution - U.S. Nationwide distribution in the states of AK, AL,…Official notice →
Other drugs & medical recalls in the United States
- 2023-08-02
- US
Qiagen GmbH recalls QIAstat-Dx Respiratory SARS-CoV-2 Panel -US IVD qualitative test intended for analyzing nasopharyngeal swab (NPS) samples from patients…
Identified a decreased performance reliability rate, Run abortions could cause delayed diagnosis since sample testing would have to be repeated
FDA · DeviceQiagen GmbHDC, AL, CA, FL, GA, ME, NC, NY, OR, TX Foreign: DE, AE, AT, BE, BG, CH, CL,…Official notice → - US
Davol, Inc. recalls Ventralight ST w Echo PS 4.5" Circle A low profile, bioresorbable, coated, permanent mesh, with a pre-attached removable positioning…
Balloon may not inflate as intended. If the balloon does not inflate during laparoscopic ventral hernia repair this may result in a delay or prolongation of the procedure, inadequate mesh placement, erosion/migration,…
FDA · DeviceDavol, Inc.Worldwide distribution - US Nationwide and the countries of Belgium, Czech…Official notice → - US
Siemens Medical Solutions USA, Inc recalls Cios Select VA 21 with FD- A Mobile X-ray system intended for use in Operating room, Traumatology, Endoscopy, Intensive Care…
Incorrect glue was applied on the plexiglass sheet on the single tank cover assembly could potentially fall off and the ingress of liquid may occur, the risk of electric shock exists (e.g., ingress of a large amount of…
FDA · DeviceSiemens Medical Solutions USA, IncWorldwide - US Nationwide distribution in the states of FL, GA, KS, MN, NC, NY…Official notice → - US
MICROVENTION INC. recalls FRED Flow Re-Direction Endoluminal Device, REF: FRED3507-PMA, FRED3511, FRED3511-PMA, FRED3516-CA, FRED3516-PMA, FRED3524, FRED3524-CA,…
Intracranial aneurysm flow diverter device may be manufactured with an incorrect inner stent length and may not perform as intended.
FDA · DeviceMICROVENTION INC.Worldwide - US Nationwide distribution including in the states of AZ, NY, FL,…Official notice → - US
Beckman Coulter, Inc. recalls Ringed DxI Reaction Vessels (RVs)
Beckman Coulter, Inc. is recalling Ringed DxI Reaction Vessels (RVs) as part of Unicel DxI Immunoassay System (600, 800 series). The reason for the recall is that the firm has identified 3 lots of RVs that failed an…
FDA · DeviceBeckman Coulter, Inc.Worldwide - US Nationwide distribution in the states of CA, MA, TX, NJ, MI,…Official notice → - US
Trexo Robotics Holdings Inc. recalls Trexo Device
Electrical issues that could potentially render the device non-functional, give off electromagnetic influence to surrounding equipment, and risk of burns when in use.
FDA · DeviceTrexo Robotics Holdings Inc.Worldwide distribution - US Nationwide and the countries of the Argentina,…Official notice →