Recall Z-1319-2018— Hill-Rom, Inc.
Class II · Terminated
Class II FDA medical device recall by Hill-Rom, Inc., initiated 2018-01-12, terminated 2020-06-26. FDA's recall record names no specific 510(k) clearance for this event. Product: Progressa Bed - AC-powered adjustable hospital bed. Reason: 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..
- Recalling firm
- Hill-Rom, Inc.
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2018-01-12
- Terminated
- 2020-06-26
- Firm location
- Batesville, IN, United States
Product description
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.
Data sourced from openFDA. This site is unofficial and independent of the FDA.