FDA Device recall Z-0067-2015
AC Powered adjustable bed frame
- FDA Device
- Class II
- terminated
- Published 2014-10-22
On 2014-10-22 the FDA classified a Class II recall of AC Powered adjustable bed frame by Primus Medical, citing firm received several complaints that the head deck actuator bracket had separated from the bed frame.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0067-2015 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2014-09-15 |
| Published | 2014-10-22 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Primus Medical |
| Distribution | US |
Product
AC Powered adjustable bed frame. AC powered adjustable bed frame used in nursing facilities.
Reason
Firm received several complaints that the head deck actuator bracket had separated from the bed frame.
Identifiers
| code_info | PCB900 manufactured between 09/13/2010 and 05/22/2012 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0067-2015%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.