Recall of Device Recall Infant 02 Transducer

According to U.S. Food and Drug Administration, this recall involved a device in United States that was produced by Ascent Healthcare Solutions, Inc..

What is this?

A correction or removal action taken by a manufacturer to address a problem with a medical device. Recalls occur when a medical device is defective, when it could be a risk to health, or when it is both defective and a risk to health.

Learn more about the data here
  • Type of Event
    Recall
  • Event ID
    47343
  • Event Risk Class
    Class 2
  • Event Number
    Z-1683-2008
  • Event Initiated Date
    2008-03-11
  • Event Date Posted
    2008-09-19
  • Event Status
    Terminated
  • Event Country
  • Event Terminated Date
    2012-06-29
  • Event Source
    USFDA
  • Event Source URL
  • Notes / Alerts
    U.S. data is current through June 2018. All of the data comes from the U.S. Food and Drug Administration, except for the category Manufacturer Parent Company.
    The Parent Company was added by ICIJ.
    The parent company information is based on 2017 public records.
  • Extra notes in the data
    Pulse oximeter - Product Code NLF
  • Reason
    Sterility compromised -- ascent healthcare solutions cannot validate the sterilization process for a variety of ascent healthcare solutions products.
  • Action
    A recall notification letter titled Voluntary Medical Device Recall was sent to each consignee. If you have questions about this recall on numerous reprocessed devices, contact Moira Barton-Varty at 888-888-3433, ext. 5350 or at mbarton@ascenths.com.

Device

  • Model / Serial
    Catalog No I-20; Lot No 135254
  • Product Classification
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Class II Recall - Nationwide Distribution.
  • Product Description
    Infant 02 Transducer (Nellcor) - Reprocessed Sterile device -- Pulse Oximeter.
  • Manufacturer

Manufacturer

  • Manufacturer Address
    Ascent Healthcare Solutions, Inc., 5307 Great Oak Drive, Lakeland FL 33815-3113
  • Manufacturer Parent Company (2017)
  • Source
    USFDA