Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Hill-Rom 1000 Bed Recalled by Hill-Rom, Inc. Due to Complaints have been reported for brakes disengaging when...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Hill-Rom, Inc. directly.
Affected Products
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.
Quantity: 8,737 devices
Why Was This Recalled?
Complaints have been reported for brakes disengaging when the bed is subjected to a hard jolt or force to the frame.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Hill-Rom, Inc.
Hill-Rom, Inc. has 35 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report