FDA recall Z-1319-2018

Hill-Rom, Inc. · Class II · device

Product

Progressa Bed - AC-powered adjustable hospital bed

Reason for recall

A component used within the braking system may break resulting in one or more brake pedals on the bed staying in brake or not being engaged which could result in unwanted bed movement and possible patient or user injury.

Distribution

Worldwide distribution. US nationwide, Canada, Chile, Colombia, Costa Rica, France, Hong Kong, Israel, Jamaica, Japan, Jordan, Malaysia, Mexico, Oman, Panama, Russian Federation, Saudi Arabia, Singapore, Spain, Taiwan, UAE, and UK.

Key facts

Status
Terminated
Initiation date
2018-01-12
Report date
2018-04-18
Termination date
2020-06-26
Voluntary/Mandated
Voluntary: Firm initiated
Location
Batesville, IN, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1319-2018