Device Recall PEAK

  • Modelo / Serial
    Lot Numbers: 11673,  12061,  12237,  12393,  12485
  • Clasificación del producto
  • Clase de dispositivo
    2
  • ¿Implante?
    No
  • Distribución
    Worldwide Distribution - United States including CA, CO, FL, IL, MD, MN, NV, NY, OH, OK, TN, TX, UT, and WAand the countries of Turkey and Ireland
  • Descripción del producto
    PEAK brand PlasmaBlade EXT, Tissue Dissection Device, || Catalogue Number: PS215-040; || Product is manufactured and distributed by PEAK Surgical, Palo Alto, CA || The PEAK Surgery System is indicated for the cutting and coagulation of soft tissue during General, Plastic and Reconstructive (including but not limited to skin incisions and development of skin flaps), ENT, Gynecologic, Orthopedic, Arthroscopic, Spinal and Neurological procedures.
  • Manufacturer
  • 1 Event

Fabricante

  • Dirección del fabricante
    Peak Surgical, 2464 Embarcadero Way, Palo Alto CA 94303-3313
  • Empresa matriz del fabricante (2017)
  • Comentario del fabricante
    “If our surveillance systems identify a potential performance issue, our personnel promptly evaluate the problem, including, when appropriate, conducting root cause investigations and internal testing to assess whether the product continues to meet specifications and defined performance criteria,” Medtronic told ICIJ in a statement. “In some cases, based on this evaluation, Medtronic may determine that a recall is necessary.” The company said that it communicates with healthcare providers and/or patients and provide recommendations to address such issues. Medtronic noted that these communications can include letters, emails, calls, press releases, physician notifications and social media postings, as well as informing the FDA and other regulators of the actions.
  • Source
    USFDA

3 dispositivos con un nombre similar

Más información acerca de la data acá

  • Modelo / Serial
    Lot number: B6Z4K.
  • Clasificación del producto
  • Clase de dispositivo
    2
  • ¿Implante?
    No
  • Distribución
    Worldwide Distribution.
  • Descripción del producto
    Peak SE Primer Kits (4 syringes per kit) manufactured by Ultradent Products, Inc, South Jordan, UT, Self Etch Primer. The product is contained within prefilled, labeled syringes in a transparent plastic container identified with an aqua, red, orange, blue and black label with black and blue print writing. Product code: 5135, 872.3200 KLE, liquid and powder mixture is a syringe-in-a-syringe delivery system. || The product is used for most bonding needs in restorative dentistry. Bonds chemical cure luting and chemical cure composites, namely PermaFlo DC. Peak SE does not require a separate etching step for quality adhesion. Peak SE is also conducive for bonding to: Dentin and enamel, porcelain, metal and composite.
  • Manufacturer
  • Modelo / Serial
    Lot numbers 07276AE2, 07299AE2, 07311AE2
  • Clasificación del producto
  • Clase de dispositivo
    2
  • ¿Implante?
    Yes
  • Distribución
    Product was distributed to 8 consignees in CA, OH, PA, CO, MA, and NJ.
  • Descripción del producto
    Stryker Peek Intraline Anchor, 6.5 mm, Model number 3910-400-020 || Used for tissue fixation to bone in certain areas.
  • Manufacturer
  • Modelo / Serial
    Lot numbers 07277AE2, 07292AE2
  • Clasificación del producto
  • Clase de dispositivo
    2
  • ¿Implante?
    Yes
  • Distribución
    Product was distributed to 8 consignees in CA, OH, PA, CO, MA, and NJ.
  • Descripción del producto
    Stryker Peek Intraline Anchor, 6.5 mm with Needles, Model number 3910-400-025 || Used for tissue fixation to bone in certain areas.
  • Manufacturer