Device Problems
Defective Device (2588); Device Dislodged or Dislocated (2923); Adverse Event Without Identified Device or Use Problem (2993)
|
Patient Problem
Pain (1994)
|
Event Date 08/28/2023 |
Event Type
Injury
|
Event Description
|
It was reported that the superion indirect decompression spacer (spacer) patient experienced pain due to the spacer dislodging and breaking.The patient has changed pain physicians and refused to provide any further information.
|
|
Manufacturer Narrative
|
Block d6a: approximated based on the patient stating implant took place in january.
|
|
Event Description
|
It was reported that the superion indirect decompression spacer (spacer) patient experienced pain due to the spacer dislodging and breaking.The patient has changed pain physicians and refused to provide any further information.
|
|
Manufacturer Narrative
|
Block d6a: approximated based on the patient stating implant took place in (b)(6).
|
|
Search Alerts/Recalls
|