Z-0446-03

Bed/chair alarm

Name: Z-0446-03 Bed/chair alarm
Creator: RF Technologies, Inc.
Published: 2002-12-16
License: https://open.fda.gov/license/

RF Technologies, Inc. / initiated 2002-12-16 / Terminated

FDA source

RF Technologies, Inc. began a recall of Bed/chair alarm on 2002-12-16. The reason FDA records is "In some cases the unit appears to be monitoring the patient, when in fact the alarm is silenced". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-0446-03
Status: Terminated
Initiated: 2002-12-16
Posted: 2003-01-16
Terminated: 2003-07-31
Recalling firm: RF Technologies, Inc.
Product: Bed/chair alarm
Product code: KMI Monitor, Bed Patient
Reason for recall: In some cases the unit appears to be monitoring the patient, when in fact the alarm is silenced.
FDA root cause: Other
Quantity in commerce: 113
Distribution: Nationwide
Product codes and lots: All units produced

Product code KMI

The FDA recall record names no cleared device, and no clearance has been matched to it.

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)