Bed/chair alarm
FDA device recall Z-0446-03 · posted 2003-01-16 · Terminated
Recall details
- Recalling firm
- RF Technologies, Inc.
- Reason for recall
- In some cases the unit appears to be monitoring the patient, when in fact the alarm is silenced.
- Root cause
- Other
- Status
- Terminated
- Product code
- KMI
- Quantity affected
- 113
- Distribution
- Nationwide
- Date initiated
- 2002-12-16
- Date posted
- 2003-01-16
- Date terminated
- 2003-07-31
- Location
- Brookfield, WI
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