FDA Device recall Z-1466-2013
Hill-Rom 1000 Bed, Product No. P1160
- FDA Device
- Class II
- terminated
- Published 2013-06-12
On 2013-06-12 the FDA classified a Class II recall of Hill-Rom 1000 Bed, Product No. P1160 by Hill Rom, citing complaints have been reported for brakes disengaging when the bed is subjected to a hard jolt or force to the frame.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1466-2013 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2013-04-15 |
| Published | 2013-06-12 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Hill Rom |
| Distribution | US |
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.
Identifiers
| code_info | Product number (P1160) with Serial Numbers J143AP0937 thru O080AP5661. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
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Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1466-2013%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.