FDA recall notice
Outpatient Telemetry Correction: Philips Issues Correction for Monitoring Service…
FDA Recall Confirmed · Mobile Cardiac Telemetry Monitoring · posted Jan 13, 2025
Key facts
| Notice | Outpatient Telemetry Correction: Philips Issues Correction for Monitoring Service Application used with Mobile Cardiac Outpatient Telemetry Due to Potential for Missed Information or Notifications That May Impact Patient Care |
|---|---|
| Device type | Mobile Cardiac Telemetry Monitoring |
| Status | Recall Confirmed |
| Posted | Jan 13, 2025 |
| Notice on fda.gov | fda.gov |
At a glance
- Confirmed Recall confirmed
- Yes Currently listed by the FDA
- None Recall events referenced
- None UDI device identifiers named
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recall notices and early alerts
The FDA's Medical Device Recalls and Early Alerts list covers the most serious device recalls, plus early alerts about potentially high-risk device issues while the FDA is still collecting information. A notice is updated as the recall is confirmed or changes.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls and Early Alerts · Source date: