Model Number N/A |
Device Problem
Appropriate Term/Code Not Available (3191)
|
Patient Problems
Headache (1880); Dizziness (2194)
|
Event Date 04/14/2016 |
Event Type
Injury
|
Manufacturer Narrative
|
This report is filed april 14, 2016.The device is currently unavailable.
|
|
Event Description
|
Per the clinic, the patient experienced headaches and dizziness with the device.Subsequently on (b)(6) 2016, the device was explanted.
|
|
Manufacturer Narrative
|
Correction: the correct patient identifier is (b)(6); not (b)(6) as previously reported.Correction: the correct catalog # is 93331; not 93329 as previously reported.
|
|
Search Alerts/Recalls
|