Drugs & medicalClass II

Technomed Europe recalls Disposable Subdermal Needle Electrode, Pt/lr, 12 x 0.40mm, product number TE/S46/638, 25 needles per package, sterile.

Burns of varying degrees can occur to patients with electrodes left in while in the MRI scanner as a result of inadequate safety information in the IFU.

Read the official notice →
Date
2022-09-21
Country
United States
Brand
Technomed Europe
Product
Disposable Subdermal Needle Electrode, Pt/lr, 12 x 0.40mm, product number TE/S46/638, 25 needles per package, sterile.
Classification
Class II
Units
US Nationwide distribution in the states of CA, FL, NH, OH, and WA.
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 Details may be shortened or out of date; the official notice is the authoritative source.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 Technomed Europe recalls

  1. 2024-09-18
  2. US
    Drugs & medicalClass II

    Technomed Europe recalls NEUROSIGN Disposable Stimulating Dissector, REF 5888-00

    Product has have presence of brown discoloration or substance on the hinge area of the device

    FDA · DeviceTechnomed EuropeUS: FL, CA, TX, IL, NY, PA, MAOfficial notice →
  3. 2022-01-19
  4. US
    Drugs & medicalClass II

    Technomed Europe recalls Disposable Subdermal Needle Electrode, Corkscrew, Single Use, Sterile; Model Numbers TE/S50715-001-C, TE/S50725-001C, and TE/S50715-001.

    There is a high risk of the blue hub detaching from the corkscrew needle, resulting the the needle remaining in the patient's scalp.

    FDA · DeviceTechnomed EuropeUS Nationwide distribution in the states of California, Florida, and Ohio.Official notice →
All 3 Technomed Europe recalls →

Other drugs & medical recalls in the United States

  1. 2022-09-21
  2. US
    Drugs & medicalClass III

    Polymer Technology Systems, Inc. dba PTS Diagnostics, Inc. recalls PTS Panels CHOL+GLU Test Strips (REF 1765)

    Incorrect instructions for use were packaged into the final product.

    FDA · DevicePolymer Technology Systems, Inc. dba PTS Diagnostics, Inc.Worldwide distribution - US Nationwide distribution in the state of Virginia…Official notice →
  3. US
    Drugs & medicalClass III

    Microbiologics Inc recalls Helix Elite Inactivated Standard, labeled as: a. Inactivated SARS-CoV-2 B.1.1.7 Whole Virus, REF HE0071N; b. Inactivated SARS-CoV-2…

    Product not registered for use in the UK

    FDA · DeviceMicrobiologics IncInternational distribution to the country of United Kingdom.Official notice →
  4. US
    Drugs & medicalClass II

    Isopure Corp recalls Acidified Concentrate Distribution and Storage-The Isopure ACDS (Acidified Concentrate Distribution and Storage) with remote fill is…

    Acidified Concentrate Distribution System potential electrical safety hazard may result in electric shock, arching

    FDA · DeviceIsopure CorpUS Nationwide distribution.Official notice →
  5. US
    Drugs & medicalClass III

    Steris Corporation Hopkins Facility recalls Verify SixCess Challenge Pack. Used to confirm that critical parameters of steam sterilization have been reached within a…

    Product contains incorrect chemical indicators in packaging.

    FDA · DeviceSteris Corporation Hopkins FacilityDistribution in the US only - AK, AR, AZ, CA, CO, FL, GA, IA, ID, IL, IN, KY,…Official notice →
  6. US
    Drugs & medicalClass II

    Mako Surgical Corporation recalls Stryker USB Converter, Polaris Spectra Camera, Catalog #201148, a component of the Mako Robotic-Arm Assisted Surgery System.

    Certain units have the potential to exhibit infant failures whereby units either arrive non-functional, have the potential to become non-functional, or flash an error light while in use.

    FDA · DeviceMako Surgical CorporationUS Distribution was made to IL and AZ.Official notice →
  7. US
    Drugs & medicalClass II

    Exactech, Inc. recalls GXL acetabular liners, orthopedic hip implant component. Product Line Numbers: a. ACUMATCH GXL 0 DEGREE LINER 28MM SZ E, REF 130-28-25 b.…

    Specific GXL acetabular polyethylene liners, packaged in non-conforming bags, may adversely impact the device and contribute to accelerated wear.

    FDA · DeviceExactech, Inc.Worldwide distribution: US (nationwide) and OUS (foreign) countries of:…Official notice →
See all drugs & medical recalls →