CLASS II Device recall · Reported 10 Oct 2012 · FDA Enforcement Report

Tabs Professional Monitor, without wall bracket recalled

Stanley Security Solutions is recalling Tabs Professional Monitor, without wall bracket, distributed nationwide in the US. The recall was initiated on 4 May 2012 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesSerial numbers 236662 thru 265692
Quantity recalled4,749 units

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

Recall details

Recall number
Z-2489-2012
FDA event ID
61796
Recalling firm
Stanley Security Solutions, Lincoln, NE
Classification
Class II
Status
Terminated
Recall initiated
4 May 2012
FDA classified
28 Sep 2012
Reported
10 Oct 2012
Type
Voluntary: Firm initiated
Customers notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category
Device Malfunction
Device type
Patient Monitors

Timeline

4 May 2012Recall initiated by company
28 Sep 2012Classified by FDA+147 days
10 Oct 2012Published in enforcement report+12 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

The monitor may fail to sound an alarm

Device recalls are issued when a component, software or design fault could cause the device to fail or give wrong readings. Many are corrections applied in the field rather than physical returns.

Product as listed by the FDA

Tabs Professional Monitor, without wall bracket, Model 25023. Stanley Security Solutions, Inc., Lincoln, NE. Designed to help reduce the risk of falls by alerting caregivers when a resident is leaving a bed, chair, room or wheelchair.

Where it was distributed

Worldwide Distribution - USA (nationwide) and the countries of Canada and Great Britain.

Nationwide

Questions about this recall

Why was it recalled?

The monitor may fail to sound an alarm

Which lots are affected?

Serial numbers 236662 thru 265692

Where was it sold?

Worldwide Distribution - USA (nationwide) and the countries of Canada and Great Britain.

What should I do if I have it?

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

Other products in this recall event

4 other products · FDA event 61796

This product is part of a recall event; the main page for the event is Tabs Professional Monitor, without pull cord or wall bracket recalled.

More recalls from Stanley Security Solutions

All 9

Other Patient Monitors recalls

All 1,013