Trinica® Trinica® 07.00119.008Recalls & reported problems
Zimmer Spine, Inc. · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00889024321281), received between Feb 17, 2023 and Feb 17, 2023 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Packaging Problem” (2 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.
Most reported problems
Device problems
- Packaging Problem2
Patient problems
- No Clinical Signs, Symptoms or Conditions2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionFeb 17, 2023Packaging Problem; Packaging Problem
IT WAS REPORTED THAT TWO BAGS LABELED AS TRINICA SELF-TAPPING FIXED SCREWS ACTUALLY CONTAINED SELF-DRILLING VARIABLE SCREWS. THESE WERE IDENTIFIED UPON RECEIPT SO THERE WAS NO PATIENT INVOLVEMENT. THIS IS REPORT TWO OF TWO FOR THIS EVENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16399566 ↗MalfunctionFeb 17, 2023Packaging Problem; Packaging Problem
IT WAS REPORTED THAT TWO BAGS LABELED AS TRINICA SELF-TAPPING FIXED SCREWS ACTUALLY CONTAINED SELF-DRILLING VARIABLE SCREWS. THESE WERE IDENTIFIED UPON RECEIPT SO THERE WAS NO PATIENT INVOLVEMENT. THIS IS REPORT ONE OF TWO FOR THIS EVENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16399551 ↗
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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
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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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