Trestle Luxe 71001-020Recalls & reported problems
Alphatec Spine, Inc. · ANTERIOR CERVICAL PLATE ASSEMBLY, 1-LEVEL, 020mm · Class 2 · Implant
All models of Trestle Luxe (24)
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 00844856066922), received between Jun 8, 2018 and Feb 7, 2019 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Bent” (1 report).
2 other recalls cover devices cleared under the same FDA submission (K102820); they may or may not involve this specific model.
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
- Bent1
- Detachment Of Device Component1
- Material Twisted/Bent1
Patient problems
- No Consequences Or Impact To Patient1
- No Information1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionFeb 7, 2019Material Twisted/Bent
PLATE BACKED OFF AS SURGEON WAS INSERTING THE SCREWS. IN THE PROCESS THE LOCKING MECHANISM GOT BENT AND NO LONGER FUNCTIONAL. NO PATIENT HARM.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 8315742 ↗MalfunctionJun 8, 2018Bent; Detachment Of Device Component
DURING THE SURGERY, THE PLATE WAS COMING OFF THE BONE AS THE SURGEON WAS ATTEMPTING TO INSERT THE SCREWS. IN THE PROCESS, THE LOCKING MECHANISM GOT BENT AND BECAME NONE FUNCTIONAL.
Patient problems: No Information
MAUDE report 7582196 ↗
Recalls under the same FDA submission
These recalls involve devices cleared under K102820. One submission often covers many models, so check the product and lot details in each record.
- Z-1547-2015 · Apr 10, 2015 · Terminated4.0mm Variable Angle, Self-Drilling Hexalobe Screw, 14mm Alphatec Spine Solutions for the Aging Spine Trestle Luxe Anterior Cervical Plating System REF 71240-14 LOT XXXXXX Alphat
- Z-2273-2012 · May 29, 2012 · TerminatedTRESTLE LUXE Anterior Cervical Plating System, Product code KWQ. 510(k) K102820. The TRESTLE LUXE Anterior Cervical Plating System is a temporary device used to stabilize the cerv
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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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