JULIET ® Ti LL JLT-MX 50 14-SRecalls & reported problems
SpineArt SA · LATERAL LUMBAR TI-LIFE CAGE · Class 2 · Implant
All models of JULIET Ti LL (13)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 07640178987074), received between Jul 12, 2024 and Jul 12, 2024 — classified as 1 injury.
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.
Reports received per month
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem1
Patient problems
- Hernia1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryJul 12, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
ON 17.MAY.2024, WE RECEIVED A COMPLAINT FROM THE FIELD (SEE CPT-2996 FOLDER), FROM FRANCE, REPORTING THAT, AFTER A SURGERY REALIZED ON (B)(6) 2022, THE PATIENT STARTED TO HAVE PAIN WITH SLIGHT LAMENESS WHEN WALKING IN THE RIGHT LOWER LIMB, TRUNCATED IN THE THIGH, RATHER ON THE ANTERO-LATERAL SIDE, SINCE (B)(6) 2022. THE ACTION TAKEN AT THIS TIME WERE HIP X-RAY ASSESSMENT, MRI ASSESSMENT THEN CONSULTATION. ON 03.JUN.2024, WE RECEIVED ADDITIONAL INFORMATION. THE PATIENT STARTED TO HAVE PERSISTENT LUMBORADICULAR PAIN IN THE RIGHT LOWER LIMB, TYPICAL SCIATICA, INCREASINGLY INCAPACITATING MECHANICS SINCE 01.DEC.2023. A LUMBAR MRI AND INFILTRATION WERE REALIZED. A DISCAL HERNIA AT ADJACENT SEGMENT L5/S1 WAS DETECTED. THE PATIENT UNDERWENT A NEW INTERVENTION ON (B)(6) 2024 (LUMBAR DISCECTOMY, NO EXPLANTATION).
Patient problems: Hernia
MAUDE report 19728087 ↗
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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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