FDA Device recall Z-1864-2012
Advanta 2 Bed
- FDA Device
- Class II
- terminated
- Published 2012-07-04
On 2012-07-04 the FDA classified a Class II recall of Advanta 2 Bed by Hill Rom, citing during an evaluation of Advanta 2 siderail samples returned from the field it was found that the screws used to attach the siderail were being stripped from the plastic cavity of….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1864-2012 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2012-06-18 |
| Published | 2012-07-04 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Hill Rom |
| Distribution | US |
Product
Advanta 2 Bed. The Advanta 2 Bed is intended for low to moderate acuity patients in the medical/surgical area of the hospital.
Reason
During an evaluation of Advanta 2 siderail samples returned from the field it was found that the screws used to attach the siderail were being stripped from the plastic cavity of the siderail.
Identifiers
| code_info | AdvantaTM 2 beds (P1190) produced between August 10, 2009 and October 6, 2011; bed S/N between K222AT9180 and M279AT4403 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Other recalls by Hill Rom
- (1)Traverse Rail Carrier E-System, wide 31017XX component to Liko overhead lift, (2)Traverse Rail Carrier 31025XX component to Liko overhea…
FDA Device · Class II · 2022-03-23 · Hill Rom - Liko Mobile Lifts: Primarily intended for use in nursing homes LikoM230 Model: 2050015
FDA Device · Class II · 2022-02-23 · Hill Rom - Liko Mobile Lifts: Primarily intended for use in nursing homes Liko M220, Model 2050010
FDA Device · Class II · 2022-02-23 · Hill Rom - These are communication systems, labeled as: a. NaviCare Nurse Call, Part Numbers: 3.6, 3.7, 3.9 b. Voalte Nurse Call, Part Number 4.0 *Pro…
FDA Device · Class II · 2021-12-29 · Hill Rom - LikoStretch 1900 Model Number: 3156051 - The combination of this products allows the user to easily adjust/control the center of gravity du…
FDA Device · Class II · 2021-10-06 · Hill Rom
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1864-2012%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.