ANTERIOR CERVICAL PLATE, MANUFACTURER UNKNOWN
Report
- Report Number
- 0009617544-2020-00087
- Event Type
- Malfunction
- Date Received
- June 17, 2020
- Date of Event
- May 21, 2020
- Report Date
- August 28, 2020
- Manufacturer
- STRYKER SPINE-US
- Product Code
- KWQ
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- US
- Reporter Occupation
- OTHER
Narratives
STRYKER MARKETING EMPLOYEE BECAME AWARE OF X-RAYS SHOWING SPINE HARDWARE FAILURE THROUGH A FACEBOOK GROUP. MULTIPLE ATTEMPTS WERE MADE TO IDENTIFY WHAT DEVICES WERE IMPLANTED AND ANY ADDITIONAL INFORMATION REGARDING THE EVENT HOWEVER NO RESPONSE WAS RECEIVED. WE ARE NOT ABLE TO CONFIRM AT THIS TIME IF ANY OF THE IMPLANTS WERE MANUFACTURED BY STRYKER. IT IS UNKNOWN IF THE PATIENT WAS HARMED AS A RESULT OF THIS INCIDENT. THE X-RAYS WERE EVALUATED BY STRYKER CHIEF MEDICAL OFFICER WHO CONCLUDED: THE PATIENT APPEARS TO HAVE BEEN IMPLANTED WITH A PLATE ON THE ANTERIOR SURFACE OF THE CERVICAL SPINE AND WITH SCREWS AND RODS ON THE POSTERIOR SURFACE OF THE CERVICAL SPINE. THE DEVICES ARE INTACT. HOWEVER, IT APPEARS THAT THE PROXIMAL SCREWS IN THE POSTERIOR CERVICAL SPINE HAVE PULLED OUT, A KYPHOTIC DEFORMITY HAS OCCURRED, AND THE PROXIMAL SCREWS IN THE ANTERIOR PLATE HAVE MIGRATED AND THE STRUT GRAFT DISLODGED. THE FAILURE OF THE SURGERY MAY BE DUE TO NUMEROUS FACTORS: INJURY POSTOPERATIVELY SUCH AS A FALL, POOR SURGICAL TECHNIQUE AND JUDGEMENT, POOR BONE QUALITY, FAILURE OF POST OPERATIVE IMMOBILIZATION. THE ROOT CAUSE OF THE EVENT CANNOT BE DETERMINED CONCLUSIVELY AS INSUFFICIENT INFORMATION WAS PROVIDED TO STRYKER. FURTHERMORE, IT CANNOT BE DETERMINED IF IMPLANTED DEVICES WERE MANUFACTURED BY STRYKER THEREFORE NO FURTHER ACTION IS REQUIRED AT THIS TIME. IF ADDITIONAL INFORMATION BECOMES AVAILABLE, THIS COMPLAINT WILL BE REOPENED AND UPDATED.
IT WAS REPORTED THROUGH SOCIAL MEDIA THAT AN UNIDENTIFIED PATIENT EXPERIENCED AN UNKNOWN EVENT INVOLVING DEVICES MADE BY AN UNIDENTIFIED MANUFACTURER. NO FURTHER INFORMATION HAS BEEN PROVIDED AT THIS TIME. THE PATIENT APPEARS TO HAVE BEEN IMPLANTED WITH A PLATE ON THE ANTERIOR SURFACE OF THE CERVICAL SPINE AND WITH SCREWS AND RODS ON THE POSTERIOR SURFACE OF THE CERVICAL SPINE. UPON PROFESSIONAL REVIEW OF THE POSTED X-RAY, IT HAS BEEN DETERMINED THAT THE DEVICES ARE INTACT. HOWEVER, IT APPEARS THAT THE PROXIMAL SCREWS IN THE POSTERIOR CERVICAL SPINE HAVE PULLED OUT, A KYPHOTIC DEFORMITY HAS OCCURRED, AND THE PROXIMAL SCREWS IN THE ANTERIOR PLATE HAVE MIGRATED AND THE STRUT GRAFT DISLODGED. THIS REPORT WILL CAPTURE THE PLATE IMPLANTED ON THE ANTERIOR SURFACE OF THE CERVICAL SPINE.
IMPLANT STATUS OF THE DEVICE IS UNKNOWN.
IT WAS REPORTED THROUGH SOCIAL MEDIA THAT AN UNIDENTIFIED PATIENT EXPERIENCED AN UNKNOWN EVENT INVOLVING DEVICES MADE BY AN UNIDENTIFIED MANUFACTURER. NO FURTHER INFORMATION HAS BEEN PROVIDED AT THIS TIME. THE PATIENT APPEARS TO HAVE BEEN IMPLANTED WITH A PLATE ON THE ANTERIOR SURFACE OF THE CERVICAL SPINE AND WITH SCREWS AND RODS ON THE POSTERIOR SURFACE OF THE CERVICAL SPINE. UPON PROFESSIONAL REVIEW OF THE POSTED X-RAY, IT HAS BEEN DETERMINED THAT THE DEVICES ARE INTACT. HOWEVER, IT APPEARS THAT THE PROXIMAL SCREWS IN THE POSTERIOR CERVICAL SPINE HAVE PULLED OUT, A KYPHOTIC DEFORMITY HAS OCCURRED, AND THE PROXIMAL SCREWS IN THE ANTERIOR PLATE HAVE MIGRATED AND THE STRUT GRAFT DISLODGED. THIS REPORT WILL CAPTURE THE PLATE IMPLANTED ON THE ANTERIOR SURFACE OF THE CERVICAL SPINE.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 626272 | ANTERIOR CERVICAL PLATE, MANUFACTURER UNKNOWN | APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY | KWQ | STRYKER SPINE-US |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |