Skip to the content

FDA Medical Device Recalls (openFDA)

Primus Medical LLC: AC Powered adjustable bed frame. AC powered adjustable bed frame used in nursing facilities.

Recall number
Z-0067-2015
Recalling firm
Primus Medical LLC
Product
AC Powered adjustable bed frame. AC powered adjustable bed frame used in nursing facilities.
Status
Terminated
Initiated
2014-09-15
Posted
2014-10-15
Terminated
2017-08-10
Reason
Firm received several complaints that the head deck actuator bracket had separated from the bed frame.
Root cause
Device Design
Action
Primus Medical will send a letter notifying all customers with PCB900 beds at their facility of the potential head bracket separation.
Quantity
1726
Distribution
Worldwide Distribution-USA (nationwide) including the states of CA, DE, FL, GA, IL, IN, KS, KY, MA, MN,MS, NC, NM, NV, NY, OH, PA, TN, TX, and VA, and the country of Canada.
Lot, serial or model codes
PCB900 manufactured between 09/13/2010 and 05/22/2012
510(k) numbers
not on file
PMA numbers
not on file
Product code
FNL
Firm FEI
3007538326
Firm city
Boardman
Firm state
OH
Firm country
not on file

Where this comes from

Register
FDA Medical Device Recalls (openFDA)
Publisher
U.S. Food and Drug Administration (openFDA)
File
device-recall-0001-of-0001.json.zip
sha256
b87518bfe2e8
Size
288210821 bytes
Published
2026-09-28
Read
2026-09-29T08:25:23.626Z
Source file
Source file retained · verify
Refresh due
2026-10-06

Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.

Cite as

FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28

Search this register