Coral 10-23-0130Recalls & reported problems
Seaspine Orthopedics Corporation · Inline Connector, 5.5mm to 5.5mm · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10889981030209), received between Sep 1, 2020 and Sep 1, 2020 — classified as 1 injury.
The most frequently reported specific device problem is “Mechanical Problem” (1 report).
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Most reported problems
Device problems
- Mechanical Problem1
- Noise, Audible1
Patient problems
- Failure of Implant1
- Patient Problem/Medical Problem1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjurySep 1, 2020Mechanical Problem; Noise, Audible; Mechanical Problem; Noise, Audible
THE PATIENT UNDERWENT SPINAL SURGERY ON (B)(6) 2020 CONSISTING OF SEASPINE'S THORACOLUMBOSACRAL PEDICLE SCREW CORAL SPINAL SYSTEM. THE PATIENT REPORTED THAT THE HARDWARE WAS "SQUEAKING" POSTOPERATIVELY, WHICH PROMPTED A REVISION SURGERY THAT TOOK PLACE ON (B)(6) 2020 TO REPLACE BOTH PREVIOUSLY IMPLANTED CORAL INLINE CONNECTORS. IT WAS REPORTED THAT AT THE TIME OF REVISION, THE SURGEON FOUND THAT THE CAUDAL SCREW ON THE RIGHT INLINE CONNECTOR WAS LOOSE.
Patient problems: Failure of Implant; Patient Problem/Medical Problem
MAUDE report 10480444 ↗
Other APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY devices
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- EVEREST® Spinal System 2901-10001VB Spine LLC · APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY119 reports
- ZEVO™ Anterior Cervical Plate System 7710015Medtronic Sofamor Danek, Inc. · APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY1 recall1 report
- XLP 7565050Nuvasive, Inc. · APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY1 recall0 reports
- Elegance® Anterior Cervical Plate 53430344Clariance · Appliance, Fixation, Spinal Intervertebral Body1 recall0 reports
- ATLANTIS® Anterior Cervical Plate System 876-170Medtronic Sofamor Danek, Inc. · APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY1 recall0 reports
- XLP 7565060Nuvasive, Inc. · APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY1 recall0 reports
- Elegance® Anterior Cervical Plate 53430113Clariance · Appliance, Fixation, Spinal Intervertebral Body1 recall0 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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