Model Number 00-3020 |
Device Problem
Failure of Device to Self-Test (2937)
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Patient Problem
No Clinical Signs, Symptoms or Conditions (4582)
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Event Date 06/22/2023 |
Event Type
malfunction
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Manufacturer Narrative
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Philips is in the process of obtaining additional information concerning this event and the complaint is still under investigation.A final report will be submitted once the investigation is complete.
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Event Description
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It was reported there was a dpm hardware failure failed pacer test message.There was no patient involvement.
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Manufacturer Narrative
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This complaint has been deemed a duplicate of (b)(4) already reported on mdr number (mfr report number: 3003832357-2023-00175).
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Search Alerts/Recalls
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