Hill-Rom 1000 Bed, Product No. P1160. The Hill-Rom 1000 Bed is intended for low to moderate acuity patient in the medica
FDA device recall Z-1466-2013 · posted 2013-06-05 · Terminated
Recall details
- Recalling firm
- Hill-Rom, Inc.
- Reason for recall
- Complaints have been reported for brakes disengaging when the bed is subjected to a hard jolt or force to the frame.
- Action taken
- On 4/16/2013 an URGENT MEDICAL DEVICE CORRECTION notification letter was sent to all consignees. The firm plans a visit to all facilities to correct each bed. Call Hill-Rom Technical Support at 800-445-3720 if you have any questions.
- Root cause
- Process control
- Status
- Terminated
- Product code
- FNL
- Quantity affected
- 8,737 devices
- Distribution
- 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
- Date initiated
- 2013-04-15
- Date posted
- 2013-06-05
- Date terminated
- 2017-02-07
- Location
- Batesville, IN
Monitor recalls programmatically
Recalls and clearances share one API, with change alerts when new recalls post.