Recall of Device Recall Vail 1000 Enclosed Bed System.

According to U.S. Food and Drug Administration, this recall involved a device in United States that was produced by Vail Products 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
    32055
  • Event Risk Class
    Class 1
  • Event Number
    Z-0862-05
  • Event Initiated Date
    2005-05-06
  • Event Date Posted
    2005-06-30
  • Event Status
    Terminated
  • Event Country
  • Event Terminated Date
    2011-01-05
  • 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
    Bed, Ac-Powered Adjustable Hospital - Product Code FNL
  • Reason
    Risk of patient entrapment, may result in serious injury or death.
  • Action
    The recalling firm sent consignees an urgent notification letter, dated 5/6/05.

Device

  • Model / Serial
    All serial numbers.
  • Product Classification
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Nationwide, Puerto Rico, Canada and Saudi Arabia. MA, RI, NH, ME, VT, CT, NJ, NY, PA, DE, Washington DC, VA, MD, VA, WV, NC, SC, GA, FL, AL, TN, MS, KY, OH, IN, MI, IA, WI, MN, SD, ND, MT, IL, MO, KS, NE, LA, AR, OK, TX, CO, WY, ID, UT, AZ, NM, NV, CA, HI, OR, WA, and AK.
  • Product Description
    Vail 1000 Enclosed Bed System.
  • Manufacturer

Manufacturer

  • Manufacturer Address
    Vail Products Inc, 235 1st St, Toledo OH 43605-2041
  • Source
    USFDA