Trinica® Trinica® 07.00117.001Recalls & reported problems
Zimmer Spine, Inc. · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 4
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 00889024320918), received between Feb 11, 2026 and Feb 11, 2026 — classified as 4 malfunctions.
The most frequently reported specific device problem is “Wrong Label” (4 reports).
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.
Reports received per month
Most reported problems
Device problems
- Wrong Label4
Patient problems
- No Clinical Signs, Symptoms or Conditions4
Recent adverse event reports
The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.
MalfunctionFeb 11, 2026Wrong Label
A DISTRIBUTOR REPORTED RECEIVING FOUR TRINICA 4.2X12MM SCREW PACKAGES THAT CONTAINED THE INCORRECT SCREW SIZE. THIS IS REPORT FOUR OF FOUR FOR THIS EVENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24317982 ↗MalfunctionFeb 11, 2026Wrong Label
A DISTRIBUTOR REPORTED RECEIVING FOUR TRINICA 4.2X12MM SCREW PACKAGES THAT CONTAINED THE INCORRECT SCREW SIZE. THIS IS REPORT THREE OF FOUR FOR THIS EVENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24317914 ↗MalfunctionFeb 11, 2026Wrong Label
A DISTRIBUTOR REPORTED RECEIVING FOUR TRINICA 4.2X12MM SCREW PACKAGES THAT CONTAINED THE INCORRECT SCREW SIZE. THIS IS REPORT TWO OF FOUR FOR THIS EVENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24317904 ↗MalfunctionFeb 11, 2026Wrong Label
A DISTRIBUTOR REPORTED RECEIVING FOUR TRINICA 4.2X12MM SCREW PACKAGES THAT CONTAINED THE INCORRECT SCREW SIZE. THIS IS REPORT ONE OF FOUR FOR THIS EVENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24317833 ↗
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- 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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