CLASS II Device recall · Reported 10 Oct 2012 · FDA Enforcement Report
Tabs Professional Voice + Monitor, with wire bracket recalled
Stanley Security Solutions is recalling Tabs Professional Voice + Monitor, with wire 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
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-2492-2012
- 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 2012 | Recall initiated by company | |
| 28 Sep 2012 | Classified by FDA | +147 days |
| 10 Oct 2012 | Published 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 Voice + Monitor, with wire bracket, Model 25223. 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.
Questions about this recall
Is Tabs Professional Voice + Monitor, with wire bracket recalled?
Yes. Stanley Security Solutions recalled Tabs Professional Voice + Monitor, with wire bracket on 4 May 2012. The recall is Class II and its status is Terminated. Recall number Z-2492-2012.
Why was it recalled?
The monitor may fail to sound an alarm
Which lots are affected?
Serial numbers 236348 thru 347416
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 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
More recalls from Stanley Security Solutions
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|---|---|---|---|---|---|
| Device | CLASS II | Senior Living Arial Emergency and Nurse Call Systems recalled | Stanley Security Solutions | Device Malfunction | Nationwide |
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| Device | CLASS I | Bravo CF capsule delivery device, Product Number FGS recalled | Given Imaging | Device Malfunction | Nationwide |
| Device | CLASS II | Lux-Dx, Lux-Dx II, Lux-Dx II+ Insertable Cardiac Monitor recalled | Boston Scientific | Device Malfunction | Nationwide |
| Device | CLASS II | Lux-Dx, Lux-Dx II, Lux-Dx II+ Insertable Cardiac Monitor recalled | Boston Scientific | Device Malfunction | Nationwide |
| Device | CLASS II | Lux-Dx, Lux-Dx II, Lux-Dx II+ Insertable Cardiac Monitor recalled | Boston Scientific | Device Malfunction | Nationwide |
| Device | CLASS II | IQecg Digital ECG recalled by Midmark | Midmark | Labeling Errors | Nationwide |