Events

Recall of Device Recall Spirit One AC Powered Hospital Bed

According to U.S. Food and Drug Administration, this recall involved a device in United States that was produced by Stryker Medical Division of Stryker Corporation.

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
    73131
  • Event Risk Class
    Class 2
  • Event Number
    Z-1556-2016
  • Event Initiated Date
    2015-07-02
  • Event Date Posted
    2016-04-22
  • Event Status
    Terminated
  • Event Country
    United States
  • Event Terminated Date
    2017-03-24
  • Event Source
    USFDA
  • Event Source URL
    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=143123
  • 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
    Inaccurate scale systems.
  • Action
    Stryker Corp. will initiate the recall by distributing letters on 07/21/2015 via FEDEX. Customers are asked to do the following: 1. Locate the units listed on the attached business reply form. 2. Remove these units from service. (Note: The original mattress purchased with the bed is not within scope of this action. The mattress will be compatible with your replacement option.) 3. Your Stryker Sales Representative will contact your facility to coordinate removal of the recalled beds and present replacement options. 4. Return the enclosed business reply form to your Stryker Sales Representative to confirm receipt of this notification or fax (269)488 -8691 or email productfieldaction@stryker.com 5. If you have loaned or sold any of the beds listed in this letter, please forward a copy of this notice to the new users and advise us of their new location in the space provided on the business reply form. 6. If you have disposed of any of the beds and they are no longer in use, please advise us of their obsolescence by providing us with their serial number in the space provided on the business reply form. *For additional information, please refer to the products operations and/or maintenance manuals. Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA's MedWatch Adverse Event Reporting program either online, by regular mail or by fax. If there are any questions or concerns, please contact Stryker Customer Service (1-800-327-0770) during normal business hours are Monday-Friday 8 a.m-6 p.m. (EST).

Device

Device Recall Spirit One AC Powered Hospital Bed
  • Model / Serial
    MDL#: E341062; Serial Numbers: B5A00-029643 029644 029537 029538 029539 029412 029413 029092 029093 029430 029431 029432 029433 029411 029479 029480 029463 029658 029461 029462 027773 029536 029420 029421 029423 029424 029094 029095 029096 029097 029098 029458 029459 027772 028853 028854 029563 029564 029639 029640 028835 030097 030099 028845 028846 028847 028848 029416 028003 029177 029418 029427 029428 029558 029559 029560 028834 029419 029429 029416 028840 028842 028843 028844 028836 028837 028838 028839 028849 028850 028851 028852 028841 028957 028958 028959 029460 029466 029467 029468 029415 029648 029460 029466 029645 029649 029650 029652 029654 029655 029657 029659 030096 030098 029467 029468 029656 029417 030154 030157 030158 030159 030161 030223 030225 030226 030354 030100 030152 030439; B5F00-029179 028654 028655 028656 028659 028660 028661 028663 028664 028793 028657 029540 029541 029646 029642 028788 029176 029175 029414 029178 029561 028216 029464 030151; B5C00-029182 029183 029184 029185 029186 029187 029188 029189
  • Product Classification
    General Hospital and Personal Use Devices
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Distributed in the states of AL, AZ, FL, GA, HI, IA, IL, KS, LA, MI, MN, MO, NE, NJ, OH, PA, SC, TN, and TX, and the countries of Canada and UK.
  • Product Description
    Spirit One A-C Powered Hospital Bed
  • Manufacturer
    Stryker Medical Division of Stryker Corporation

Manufacturer

Stryker Medical Division of Stryker Corporation
  • Manufacturer Address
    Stryker Medical Division of Stryker Corporation, 3800 E Centre Ave, Portage MI 49002-5826
  • Manufacturer Parent Company (2017)
    Stryker
  • Source
    USFDA