Drugs & medicalClass II

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.

Read the official notice →
Date
2024-08-21
Country
United States
Brand
Argon Medical Devices
Product
L-CATH PICC S/L Peripherally Inserted Central Catheter, 26Ga (1.9F) 0.60mm x 30cm, REF: 384539
Classification
Class II
Units
US distribution to the states of: TX, WA, CA, IL
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 Details may be shortened or out of date; the official notice is the authoritative source.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

  1. Check the product name, strength and lot number against the official notice.
  2. Do not stop a prescribed medicine without talking to your doctor or pharmacist first.
  3. 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

  1. 2026-07-22
  2. US
    Drugs & medicalClass I

    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 →
  3. 2025-12-03
  4. US
    Drugs & medicalClass II

    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 →
  5. 2024-10-02
  6. US
    Drugs & medicalClass II

    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 →
  7. 2023-08-02
  8. US
    Drugs & medicalClass II

    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 →
  9. 2022-02-16
  10. US
    Drugs & medicalClass II

    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 →
  11. 2021-12-15
  12. US
    Drugs & medicalClass II

    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 →
All 8 Argon Medical Devices recalls →

Other drugs & medical recalls in the United States

  1. 2024-08-28
  2. US
    Drugs & medicalClass II

    Teva Pharmaceuticals USA, Inc recalls Testosterone Gel, 1.62%, (Alcohol 80% v/v), 30 unit-dose packets, Rx Only, Teva Pharmaceuticals, USA, Inc. North Wales, PA 19454,…

    Superpotent Drug

    FDA · DrugTeva Pharmaceuticals USA, IncProduct was distributed nationwide within the United StatesOfficial notice →
  3. US
  4. US
    Drugs & medicalClass I

    Hikma Pharmaceuticals USA Inc. recalls Acetaminophen Injection, 1,000 mg per 100 mL (10 mg/mL), 100 mL Single Dose bags, For Intravenous Use Only, Rx Only, Manufactured…

    Labeling: Label Mix-up: a bag of Dexmedetomidine HCl in 0.9% Sodium Chloride Injection was found inside an overwrap labeled Acetaminophen Injection 1,000 mg per 100 mL (10 mg/mL)

    FDA · DrugHikma Pharmaceuticals USA Inc.OH and PROfficial notice →
  5. 2024-08-21
  6. US
    Drugs & medicalClass III

    DRG International, Inc. recalls Product Name: Salivary Testosterone ELISA Model/Catalog Number: SLV-3013 Product Description: An enzyme immunoassay for the quantitative…

    Invalid Controls. The Low Control is out of range; too high which causes invalid runs that would result in repeating the runs and delays for reporting results to patients.

    FDA · DeviceDRG International, Inc.US Nationwide distribution in the states of CA, IL, MN, PA, UT, VA.Official notice →
  7. US
    Drugs & medicalClass II

    DKK Dai-Ichi Shomei Co., Ltd. recalls Aurora Series, Aurora 7 lighthead; Models: LED7 (including TV models). The Aurora Series is intended to illuminate the surgical…

    The weld on the light head frame can crack which could lead to problems such as the light head frame sagging, the plastic front face housing cracking, or the light head detaching.

    FDA · DeviceDKK Dai-Ichi Shomei Co., Ltd.Domestic: Nationwide Distribution International: Australia, Canada, Egypt,…Official notice →
  8. US
    Drugs & medicalClass II

    Boston Scientific Neuromodulation Corporation recalls WAVEWRITER ALPHA: Model: SC-1216, 16 IPG KIT, REF: M365SC12160; Model: SC-1232, 32 IPG KIT, REF: M365SC12320

    Spinal Cord Stimulation (SCS) Implantable Pulse Generator (IPG) may experience routine system check during IPG charging, which may cause device reset, which may lead to transient loss of stimulation; patients may…

    FDA · DeviceBoston Scientific Neuromodulation CorporationWorldwide Distribution: US (nationwide) including states of: TN, PA, WA, SC,…Official notice →
See all drugs & medical recalls →