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Hill-Rom, Inc. recalls Hill-Rom 1000 Bed, Product No. P1160. The Hill-Rom 1000 Bed is intended for low to moderate acuity patient in the medi
Recalled June 12, 2013 · FDA recall Z-1466-2013 · Hill-Rom
Hazard
Complaints have been reported for brakes disengaging when the bed is subjected to a hard jolt or force to the frame. · FDA Class II
Units
8,737 devices
Sold at
Worldwide distribution: US (Nationwide) and countries of: Argentina , Bahamas, Bahrain, Bolivia, Brazil, Canada, Chile, China, Colombia, Costa Rica, Ecuador, Egypt, Ethiopia, France, Ghana, Guam, Hong Kong, India, Indonesia, Japan, Jordan, Kuwait, Lebanon, Libya, Malaysia, Mexico, N. Mariana Islands, Pakistan, panama, Paraguay, Puerto Rico, Qatar, Saudi Arabia, Singapore, South Africa, South Korea, Taiwan, Thailand, United Arab Emirates, United States, US Virgin Islands, Venezuela and Vietnam.
Description
Complaints have been reported for brakes disengaging when the bed is subjected to a hard jolt or force to the frame.
Product
Hill-Rom 1000 Bed, Product No. P1160. The Hill-Rom 1000 Bed is intended for low to moderate acuity patient in the medical surgical area of the hospital.
Manufacturer(s)
Hill-Rom, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →