Drugs & medicalClass I

Inari Medical - Oak Canyon recalls ClotTriever XL Catheter, 30 mm, REF: 41-102, used with Instructions for Use ClotTriever XL Catheter ClotTriever Thrombectomy System,…

Thrombectomy system catheter instructions for use updated to reduce adverse events due to the following circumstances: 1) Fibrous, firmly adherent, calcified material, or suspected tumor thrombus overloading catheter…

Read the official notice →
Date
2024-08-28
Country
United States
Brand
Inari Medical - Oak Canyon
Product
ClotTriever XL Catheter, 30 mm, REF: 41-102, used with Instructions for Use ClotTriever XL Catheter ClotTriever Thrombectomy System,…
Classification
Class I
Units
Worldwide - US Nationwide distribution including in the states of PA, FL, GA,…
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 Details may be shortened or out of date; the official notice is the authoritative source.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 Inari Medical - Oak Canyon recalls

  1. 2025-05-14
  2. US
    Drugs & medicalClass II

    Inari Medical - Oak Canyon recalls Artix MT Thrombectomy Device, REF: 32-102

    Thrombectomy device specifies vessel range of 2.5-6 mm on the pouch, carton, and Instructions for Use rather than the correct vessel range of 3-6 mm, which could incrementally increase the radial force on the artery,…

    FDA · DeviceInari Medical - Oak CanyonUS Nationwide distribution in the states of FL, IL, WI, KY, TX, CA, OH, GA,…Official notice →
All 2 Inari Medical - Oak Canyon recalls →

Other drugs & medical recalls in the United States

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

    Ventana Medical Systems, Inc. recalls Ventana anti-CD10 (SP67) Rabbit Monoclonal Primary Antibody, REF: 790-4506, IVD

    Their is a potential for high background and off-target staining when using the monoclonal primary antibody which can result in false positive results.

    FDA · DeviceVentana Medical Systems, Inc.Worldwide - US Nationwide distribution including in the states of AK, AL, AR,…Official notice →
  3. US
    Drugs & medicalClass II

    Microtek Medical Inc. recalls Bag Decanter II, REF 2002S. Packaged on a form, fill and seal machine with a poly/Tyvek material then placed 50 products to a case (cs).

    During sterile barrier testing performed on the decanter product line, the samples were identified to have pin holes and tears in the packaging film.

    FDA · DeviceMicrotek Medical Inc.Distributed nationwide and internationally to Canada, Mexico, New Zealand,…Official notice →
  4. US
    Drugs & medicalClass I

    Covidien recalls McGrath Mac Video Laryngoscope, REF: 300-000-000 , Non-Sterile, Rx Only

    Battery management system within Laryngoscope devices may deplete below the deign threshold which may result in thermal event followed by risk of explosion.

    FDA · DeviceCovidienWorldwide - US Nationwide distribution including in the states of AK, AL, AR,…Official notice →
  5. US
    Drugs & medicalClass II

    Baxter Healthcare Corporation recalls Spectrum Wireless Battery Modules A/B/G/N, product code 36010, used with either of the following 35700BAX2 (Spectrum V8 infusion…

    The Spectrum WBM may fail to auto-document infusion status information back to the hospital's Electronic Medical Record (EMR) system. This software issue only impacts customers where the Spectrum V8 or Spectrum IQ…

    FDA · DeviceBaxter Healthcare CorporationUS, NationwideOfficial notice →
  6. US
    Drugs & medicalClass II

    FDC Limited recalls Timolol Maleate Ophthalmic Solution USP, 0.5%, packaged in: a) 5mL bottle (NDC 64980-514-05), and b) 10mL bottle (NDC 64980-514-01), Rx…

    Defective Container: patients are unable to get the solution out of the bottle as the spike of the cap was lodged in the nozzle of the product bottle.

    FDA · DrugFDC LimitedNationwide U.S.A.Official notice →
  7. US
    Drugs & medicalClass I

    Aurobindo Pharma USA Inc recalls Healthy Living Acetaminophen, Aspirin (NSAID) and Caffeine, tablets USP, 250 mg/250 mg/65 mg, 100-count bottles, Distributed by:…

    Labeling: Missing Label - some bottles are missing the the manufacturers label that includes the drug facts information.

    FDA · DrugAurobindo Pharma USA IncNJ, NY & PAOfficial notice →
See all drugs & medical recalls →