Trestle Luxe 71240-14Recalls & reported problems
Alphatec Spine, Inc. · 4.0mm Variable Angle, Self-Drilling Hexalobe Screw, 14mm · Class 2 · Implant
All models of Trestle Luxe (24)
Data updated Oct 16, 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 00844856067325), received between May 22, 2017 and May 22, 2017 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Break” (2 reports).
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 16, 2026.
Most reported problems
Device problems
- Break2
Patient problems
- No Information2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionMay 22, 2017Break
PATIENT RETURNED FOR A 3 MONTH POST-OP VISIT AND X-RAYS TAKEN AT THE TIME FOUND TWO BROKEN 14MM SELF-DRILLING SCREWS. THE TRESTLE LUXE PLATING SYSTEM WAS ORIGINALLY IMPLANTED ON (B)(6) 2016.
Patient problems: No Information
MAUDE report 6581640 ↗MalfunctionMay 22, 2017Break
PATIENT CAME IN FOR 1 YEAR VISIT. X-RAY'S SHOW THE TWO BOTTOM SCREWS SNAPPED IN HALF. THE TRESTLE LUXE PLATING SYSTEM WAS ORIGINALLY IMPLANTED ON (B)(6) 2016.
Patient problems: No Information
MAUDE report 6581361 ↗
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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- ZEVO™ Anterior Cervical Plate System 7710015Medtronic Sofamor Danek, Inc. · APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY1 recall1 report
- Mariner RDX MX1-000040Seaspine Orthopedics Corporation · Appliance, fixation, spinal intervertebral body1 recall0 reports
- Mariner RDX MX1-000030Seaspine Orthopedics Corporation · Appliance, fixation, spinal intervertebral body1 recall0 reports
- Elegance® Anterior Cervical Plate 53430112Clariance · Appliance, Fixation, Spinal Intervertebral Body1 recall0 reports
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- XLP 7565050Nuvasive, Inc. · 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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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