Recall Z-1466-2013— Hill-Rom, Inc.
Class II · Terminated
Class II FDA medical device recall by Hill-Rom, Inc., initiated 2013-04-15, terminated 2017-02-07. FDA's recall record names no specific 510(k) clearance for this event. 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.. Reason: Complaints have been reported for brakes disengaging when the bed is subjected to a hard jolt or force to the frame..
- Recalling firm
- Hill-Rom, Inc.
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2013-04-15
- Terminated
- 2017-02-07
- Firm location
- Batesville, IN, United States
Product description
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.
Reason for recall
Complaints have been reported for brakes disengaging when the bed is subjected to a hard jolt or force to the frame.
Data sourced from openFDA. This site is unofficial and independent of the FDA.