Z-1944-2010

Tabs Professional Monitor, includes one wall bracket, Model 25022. Stanley Senior Technologies, Lincoln, NE

Name: Z-1944-2010 Tabs Professional Monitor, includes one wall bracket, Model 25022. Stanley Senior Technologies, Lincoln, NE
Creator: Stanley Security Solutions, Inc.
Published: 2010-03-26
License: https://open.fda.gov/license/

Securitas Healthcare LLC / initiated 2010-03-26 / Terminated

FDA source

Stanley Security Solutions, Inc. began a recall of Tabs Professional Monitor, includes one wall bracket, Model 25022. Stanley Senior Technologies, Lincoln, NE on 2010-03-26. The reason FDA records is "Product might not indicate low battery alarms or exit alarms when powered by a DC power supply". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-1944-2010
Status: Terminated
Initiated: 2010-03-26
Posted: 2010-07-01
Terminated: 2011-09-16
Recalling firm: Securitas Healthcare LLC
Product: Tabs Professional Monitor, includes one wall bracket, Model 25022. Stanley Senior Technologies, Lincoln, NE.
Product code: KMI Monitor, Bed Patient
Reason for recall: Product might not indicate low battery alarms or exit alarms when powered by a DC power supply.
FDA root cause: Component change control
Action: The firm made phone calls beginning 3/26/10 to customers who purchased the 12-volt power supply informing them of the recall and instructing them to determine the number of units that will need to be returned for replacement. Important Safety Notice letters dated 3/25/10 were issued via regular mail on 3/26/10 and also providing the reason for the recall, instructions, and customer service contact information to arrange for return of the units.
Quantity in commerce: 84 units
Distribution: Nationwide Distribution
Product codes and lots: Serial numbers 235388 thru 237658.

Product code KMI

K873806Class IJdm Sp2 SensorJd Monitoring C/O Mackler, Cooper and Gibbs / cleared 1987-12-08

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device recall database and the FDA enforcement reports, both ingested from openFDA. The recall record supplies the product, the reason and the product code; the enforcement report supplies the classification. The two datasets are exported by FDA on different days, and the date above is the older of the two, so nothing on this page is newer than it says.

MDM adds the root cause tag, derived from FDA’s own root cause text, and the cross-links to the product code, the clearances named on the record and MDM coverage. Where a recall has not been joined to an enforcement report, no classification is shown.

Data as of 2026-09-30, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)