Manufacturers

Hill-Rom, Inc.

21 devices in the database

Device Recall VersaCare
  • Model / Serial
    All serial numbers distributed prior to November 22, 2004.
  • Product Classification
    General Hospital and Personal Use Devices
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Nationwide.
  • Product Description
    Hill-Rom brand VersaCare Bed; product P3200.
Hill-Rom CareAssist Bed; model P1170.
  • Model / Serial
    All units shipped prior to September 22, 2004.
  • Product Classification
    General Hospital and Personal Use Devices
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Nationwide, Canada and Saudi Arabia.
  • Product Description
    Hill-Rom CareAssist Bed; model P1170.
Hill-Rom Newborn bassinet; model P247
  • Model / Serial
    All units distributed from November 2000 through April 2003.
  • Distribution
    United States, Brazil, Canada, China, Italy, Japan, Kuwait Netherlands, Qatar, United Kingdom
  • Product Description
    Hill-Rom Newborn bassinet; model P247
Hill-Rom Newborn bassinet; model P248
  • Model / Serial
    All units distributed from November 2000 through April 2003.
  • Distribution
    United States, Brazil, Canada, China, Italy, Japan, Kuwait Netherlands, Qatar, United Kingdom
  • Product Description
    Hill-Rom Newborn bassinet; model P248
Device Recall Resident LT bed ambulatory assist bar
  • Model / Serial
    All units distributed between March 1997 and September 2003.
  • Distribution
    United States and Canada
  • Product Description
    Hill-Rom brand Resident LT bed ambulatory assist bar accessory; accessory P865A.
16 more

11 manufacturers with a similar name

Learn more about the data here

Hill-Rom, Inc.
  • Manufacturer Address
    Hill-Rom, Inc., 1069 State Road 46 E, Batesville IN 47006-7520
  • Manufacturer Parent Company (2017)
    Hill-Rom Holdings, Inc
  • Source
    USFDA
Hill-Rom, Inc.
  • Manufacturer Parent Company (2017)
    Hill-Rom Holdings, Inc
  • Manufacturer comment
    Note published by the authorities from the Netherlands: This message is a warning from the manufacturer. After placing a medical device on the market, the manufacturer is obliged to follow the device and where necessary to improve it. When there is a risk for the user, the manufacturer must take action. The manufacturer informs users and the inspection of this action with a warning (Field Safety Notice). See also medical device warnings. This is part of the supervision of medical technology
  • Source
    IGJ
Hill-Rom, Inc.
Hill-Rom, Inc.
Hill-Rom, Inc.
6 more