AC Powered Adjustable Bed (Primus) – Bracket Separation (2014)
Class II: A situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Class II recall indicates potential for temporary health effects.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
AC Powered adjustable bed frame. AC powered adjustable bed frame used in nursing facilities.
Brand
Primus Medical LLC
Lot Codes / Batch Numbers
PCB900 manufactured between 09/13/2010 and 05/22/2012
Products Sold
PCB900 manufactured between 09/13/2010 and 05/22/2012
Primus Medical LLC is recalling AC Powered adjustable bed frame. AC powered adjustable bed frame used in nursing facilities. due to Firm received several complaints that the head deck actuator bracket had separated from the bed frame.. This is a Class I recall, indicating a high risk of serious health consequences or death. Based on FDA medical device enforcement report.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Firm received several complaints that the head deck actuator bracket had separated from the bed frame.
Recommended Action
Per FDA guidance
Healthcare providers and patients should stop using the device and contact the manufacturer for further instructions. Report problems to FDA MedWatch.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026