Trinica® Trinica® 07.00812.007Recalls & 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
- 2
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00889024324053), received between Feb 9, 2021 and Feb 9, 2021 — classified as 2 injuries.
The most frequently reported specific device problem is “Unstable” (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
- Unstable2
- Fracture1
- Migration1
Patient problems
- Inadequate Osseointegration2
- No Code Available2
- Pain2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryFeb 9, 2021Fracture; Unstable; Migration; Fracture; Unstable; Migration
IT WAS REPORTED THAT A SCREW FRACTURED AND BACKED OUT POST-OP, WHICH CAUSED THE CONSTRUCT TO BE UNSTABLE AND FUSION WAS NOT ACHIEVED. ADDITIONALLY, THE CAGE WAS FOUND TO BE CRACKED. A 2-LEVEL PLATE, 6 SCREWS, AND CAGE WERE REMOVED DURING A REVISION SURGERY. THIS IS REPORT ONE OF EIGHT FOR THIS EVENT.
Patient problems: Inadequate Osseointegration; No Code Available; Pain
MAUDE report 11302473 ↗InjuryFeb 9, 2021Unstable; Unstable
IT WAS REPORTED THAT A SCREW FRACTURED AND BACKED OUT POST-OP, WHICH CAUSED THE CONSTRUCT TO BE UNSTABLE AND FUSION WAS NOT ACHIEVED. ADDITIONALLY, THE CAGE WAS FOUND TO BE CRACKED. A 2-LEVEL PLATE, 6 SCREWS, AND CAGE WERE REMOVED DURING A REVISION SURGERY. THIS IS REPORT TWO OF EIGHT FOR THIS EVENT.
Patient problems: Inadequate Osseointegration; No Code Available; Pain
MAUDE report 11302425 ↗
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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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