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Terminated

Bed/chair alarm

FDA Recall Z-0446-03 · Posted 2003-01-16

Recalling FirmRF Technologies, Inc.
Recall StatusTerminated
Product CodeKMI
Date Initiated2002-12-16
Date Terminated2003-07-31
Product Quantity113

Reason for Recall

In some cases the unit appears to be monitoring the patient, when in fact the alarm is silenced.

Root Cause

Other

Distribution Pattern

Nationwide

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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