JULIET ® Ti LL JLT-MX 60 16-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 07640178987166), received between Jun 26, 2024 and Jun 26, 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
- Abdominal Pain1
- Obstruction/Occlusion1
- Vertebral Fracture1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryJun 26, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
WE RECEIVED A COMPLAINT FROM FRANCE ON 04.JUN.2024 REPORTING 3 AVERSE EVENTS. THE PATIENT UNDERWENT A SURGERY ON (B)(6) 2022 (CAGE IMPLANTATION). FIRST ADVERSE EVENT REPORTED: EVENT START DATE: (B)(6) 2022. EVENT DESCRIPTION: INTERVENTION TO STABILIZE THE LUMBOSACRAL JUNCTION WITH ARTHRODESIS L4L5S1. L5 FRACTURED DUE TO OSTEOPOROSIS. CAGE ARE NOT REMOVED. EVENT STOP DATE: (B)(6) 2022. SECOND ADVERSE EVENT REPORTED: EVENT START DATE: (B)(6) 2022. EVENT DESCRIPTION: FLANK LATERAL INCISIONAL HERNIA: REPAIR BY ABDOMINAL WALL HERNIORRHAPHY (NO IMPLANT). ACTION TAKEN: REINTERVENTION ON (B)(6) 2022. EVENT STOP DATE: (B)(6) 2022. THIRD ADVERSE EVENT REPORTED: EVENT START DATE: NOT REPORTED. EVENT DESCRIPTION: UNDERGOING DIGESTIVE SURGERY FOR AN OCCLUSION OF THE GRAFTED INTESTINE, POSSIBLY DUE TO A FLANGE OR ADHESION FOLLOWING THE WALL SURGERY HE UNDERWENT A FEW MONTHS EARLIER. ACTION TAKEN: SURGERY, DATE UNKNOWN EVENT STOP DATE: NOT REPORTED.
Patient problems: Abdominal Pain; Obstruction/Occlusion; Vertebral Fracture
MAUDE report 19612925 ↗
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- IdentiTi 232-10-85-250Alphatec Spine, Inc. · Intervertebral fusion device with integrated fixation, lumbar1 recall5 reports
- IdentiTi 132-10-85-300Alphatec Spine, Inc. · Intervertebral fusion device with integrated fixation, lumbar1 recall3 reports
- MectaLIF Anterior 03.30.301Medacta International SA · Intervertebral Fusion Device With Integrated Fixation, Lumbar1 recall2 reports
- IdentiTi 232-10-85-350Alphatec Spine, Inc. · Intervertebral fusion device with integrated fixation, lumbar1 recall2 reports
- IdentiTi 232-11-90-350Alphatec Spine, Inc. · Intervertebral fusion device with integrated fixation, lumbar1 recall1 report
- MectaLIF Anterior 03.30.302Medacta International SA · Intervertebral Fusion Device With Integrated Fixation, Lumbar1 recall1 report
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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