Events

Recall of Device Recall Crest SpinBrush Pro.

According to U.S. Food and Drug Administration, this recall involved a device in United States that was produced by Proctor & Gamble Co.

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
    31259
  • Event Risk Class
    Class 2
  • Event Number
    Z-0593-05
  • Event Initiated Date
    2005-02-23
  • Event Date Posted
    2005-03-11
  • Event Status
    Terminated
  • Event Country
    United States
  • Event Terminated Date
    2006-04-13
  • Event Source
    USFDA
  • Event Source URL
    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=37547
  • 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
    Toothbrush, Powered - Product Code JEQ
  • Reason
    The brushes may experience head breakage when insufficently rinsed after use and when used in combination with toothpastes containing a combination baking soda, peroxide, and sodium lauroyl sarcosinate.
  • Action
    The recalling firm sent a recall letter dated 2/23/05 and dated 3/4/05.

Device

Device Recall Crest SpinBrush Pro.
  • Model / Serial
    All codes.
  • Product Classification
    Dental Devices
  • Device Class
    1
  • Implanted device?
    No
  • Product Description
    The product is refill heads for battery powered toothbrushes. Spinbrush Pro EX Soft Refill heads, UPC776687800080.
  • Manufacturer
    Proctor & Gamble Co

Manufacturer

Proctor & Gamble Co
  • Manufacturer Address
    Proctor & Gamble Co, 2 Procter And Gamble Plz, Cincinnati OH 45202-3315
  • Source
    USFDA