Drugs & medicalClass II

Focalyx Technologies, LLC. recalls Focalyx Fusion

Software device that is an accessory for image-guided interventional and diagnostic procedures involving prostate has accessories that may not function properly with Windows 10, which may cause patient harm during…

Read the official notice →
Date
2026-02-11
Country
United States
Brand
Focalyx Technologies, LLC.
Product
Focalyx Fusion
Classification
Class II
Units
Worldwide - US Nationwide distribution in the states of NY, MA, FL and the…
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 Details may be shortened or out of date; the official notice is the authoritative source.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.

Other drugs & medical recalls in the United States

  1. 2026-02-11
  2. US
    Drugs & medicalClass II

    Changchun Wancheng Bio-Electron Co., Ltd. recalls Male Fertility Sperm Test for Home Use (Cassette)

    Test strips and other tests including for near-patient testing, that require a 510(k) were distributed before they could be legally marketed to U.S. customers; devices may cause false or inaccurate diagnostic result by…

    FDA · DeviceChangchun Wancheng Bio-Electron Co., Ltd.US Nationwide distribution in the states of TX, GA, CA.Official notice →
  3. US
    Drugs & medicalClass II

    Vortex Surgical Inc. recalls Vortex Surgical TID Pharos Illuminated Depressor, VS0801B

    XXX

    FDA · DeviceVortex Surgical Inc.Worldwide Distribution: US (nationwide) to states of: AL, AR, AZ, CA, CT, FL,…Official notice →
  4. US
    Drugs & medicalClass II

    Vortex Surgical Inc. recalls Convenience Kits 1. 25GA Convenience Kit - FNX VS0644.25-FNX 2. 25GA Convenience Kit - FXX VS0644.25-FXX 3.25GA Convenience Kit - XES…

    There may be voids located in the seal of Tyvek pouches associated with identified catalog numbers and lots. A compromised sterile barrier has potential of bioburden contamination which could lead to infection.

    FDA · DeviceVortex Surgical Inc.Worldwide Distribution: US (nationwide) to states of: AL, AR, AZ, CA, CT, FL,…Official notice →
  5. US
    Drugs & medicalClass II

    Siemens Medical Solutions USA, Inc recalls NAEOTOM Alpha.Pro Software applications: syngo.CT Brain Quantification syngo.CT Vessel Hyperdensities syngo.CT ASPECTS

    To remove the software applications from certain CT systems as the applications have not received FDA 510(k) clearance.

    FDA · DeviceSiemens Medical Solutions USA, IncWorldwide distribution - US Nationwide and the countries of Canada, Costa…Official notice →
  6. US
    Drugs & medicalClass II

    Medtronic MiniMed, Inc. recalls MiniMed 780G Insulin Pump Catalog Numbers: MMT-1884 MMT-1886 With Software Version 6.60 The MiniMed 780G insulin pump is indicated for…

    A software timing and processor communication issue in MiniMed" 780G software version 6.60 may trigger Pump Error 43 and/or Pump Error 41, resulting in suspension of insulin delivery.

    FDA · DeviceMedtronic MiniMed, Inc.Worldwide - U.S. National distribution including in the states of AL, AR, AZ,…Official notice →
  7. US
    Drugs & medicalClass II

    Tornier, Inc recalls TORNIER PERFORM REVERSED PERIP SCREW 5.0MMX18MM NON STERILE, catalog number DWJ318

    A specific lot of screws is incorrectly labeled. Screws are labeled as 5.0mmx18mm but actual screws are 5.00mmx14mm. If mismatch is detected during surgery, the issue may cause a minor delay in surgery. If not detected…

    FDA · DeviceTornier, IncUS Nationwide distribution.Official notice →
See all drugs & medical recalls →