Model Number 3186 |
Device Problem
Insufficient Information (3190)
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Patient Problem
Insufficient Information (4580)
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Event Date 06/28/2021 |
Event Type
Injury
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Manufacturer Narrative
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During processing of this complaint, attempts were made to obtain complete event and patient weight.Further information was requested but not received.The results of the investigation are inconclusive since the device was not returned for analysis.Based on the information received, the cause of the reported incident could not be conclusively determined.
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Event Description
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Related manufacturer reference number: 3006705815-2021-05374, 1627487-2021-18011.It was reported that patient underwent surgical intervention on (b)(6) 2021 wherein the entire system was explanted for being nonfunctional.
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Manufacturer Narrative
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Correction: section e1: initial reporter-reporter name should have been banner estrella medical center; reporter phone number should have been (b)(6); reporter address line 1 should have been 9201 west thomas road; reporter city should have been phoenix; reporter state should have been selected arizona; reporter postal office or zip code should have been 85037.The reported event for ineffective stimulation/ipg inoperable was confirmed.The as-received ipg would not communicate due to a depleted battery.After the battery was recovered, the ipg communicated, charged, and passed functional testing to manufacturing specifications using the autotester.Unable to determine the cause of the reported event.
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Search Alerts/Recalls
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