Avenue T AT9040RRecalls & reported problems
LDR Spine Usa, Inc. · Class 1
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 03662663003049), received between Dec 21, 2020 and Dec 24, 2020 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Fracture” (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 16, 2026.
Most reported problems
Device problems
- Fracture2
Patient problems
- No Consequences Or Impact To Patient2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionDec 24, 2020Fracture; Fracture
IT WAS REPORTED THAT TWO REMOVAL HOOKS FRACTURED DURING SURGERY. THERE WERE NO REPORTED PATIENT IMPACTS ASSOCIATED WITH THIS EVENT. THIS IS REPORT ONE OF TWO FOR THIS EVENT.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 11072389 ↗MalfunctionDec 21, 2020Fracture; Fracture
IT WAS REPORTED THAT TWO REMOVAL HOOKS FRACTURED DURING SURGERY. THERE WERE NO REPORTED PATIENT IMPACTS ASSOCIATED WITH THIS EVENT. THIS IS REPORT TWO OF TWO FOR THIS EVENT.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 11047842 ↗
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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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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