Model Number 15 |
Device Problem
Unexpected Shutdown (4019)
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Patient Problem
No Clinical Signs, Symptoms or Conditions (4582)
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Event Date 12/15/2021 |
Event Type
malfunction
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Manufacturer Narrative
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Stryker evaluated the customer's device and verified the reported issue.Stryker disassembled and properly reseated all connections and cleared error log.After observing proper device operation through functional and performance testing, the device was returned to the customer for use.The cause of the reported issue could not be determined.Initial reporter email address was not provided and is therefore, left blank.
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Event Description
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The customer contacted stryker to report that their device unexpectedly shut off.In this state the device may not be able to deliver defibrillation therapy if needed.There was no patient involvement reported with the event.
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Event Description
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The customer contacted stryker to report that their device unexpectedly shut off.In this state the device may not be able to deliver defibrillation therapy if needed.There was no patient involvement reported with the event.
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Manufacturer Narrative
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Stryker determined the battery cable was not fully seated to the contact pcb.The battery cable was reseated to resolve the issue.
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Search Alerts/Recalls
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