Devices

Device Recall Advanta 2 Bed.

Model / Serial
AdvantaTM 2 beds (P1190) produced between August 10, 2009 and October 6, 2011; bed S/N between K222AT9180 and M279AT4403
Product Classification
General Hospital and Personal Use Devices
Device Class
2
Implanted device?
No
Distribution
Worldwide Distribution-USA (nationwide) and the countries of Canada, France, and Singapore.
Product Description
Advanta 2 Bed. || The Advanta 2 Bed is intended for low to moderate acuity patients in the medical/surgical area of the hospital.
Manufacturer
Hill-Rom, Inc.
1 Event
- Recall of Device Recall Advanta 2 Bed.

Manufacturer

Hill-Rom, Inc.

Manufacturer Address
Hill-Rom, Inc., 1069 State Route 46 East, Batesville IN 47006-7520
Manufacturer Parent Company (2017)
Hill-Rom Holdings, Inc
Source
USFDA

About this database

Explore more than 120,000 Recalls, Safety Alerts and Field Safety Notices of medical devices and their connections with their manufacturers.

Stories in your inbox

Do you work in the medical industry? Or have experience with a medical device? Our reporting is not done yet. We want to hear from you.

Tell us your story!

Disclaimer

Medical devices help to diagnose, prevent and treat many injuries and diseases. We are not suggesting or implying that any companies or other entities included in the International Medical Devices Database engaged in unlawful conduct or otherwise acted improperly. The same device may have different names in different countries. This database is not intended to provide medical advice and patients should check with their doctors to determine if it contains relevant information and if such information has medical implications for them.

Download the data

The International Medical Devices Database is licensed under the Open Database License and its contents under Creative Commons Attribution-ShareAlike license. Always cite the International Consortium of Investigative Journalists when using this data. You can download a raw copy of the database here.

Download all (zipped)