JULIET Ti LLRecalls & reported problems across all models
SpineArt SA · 13 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
1 open recall names at least one JULIET Ti LL model. Check whether yours is affected in the recall details, and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls
- 1
We found 13 models of JULIET Ti LL by SpineArt SA in the FDA's device registry (GUDID). Together they are named in 2 adverse event reports in the FDA's MAUDE database, received between Jun 26, 2024 and Jul 12, 2024 — classified as 2 injuries.
1 FDA recall record name at least one of these models by its device identifier, 1 still open.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works
Reports received per month, all models
JULIET Ti LL recalls
FDA recall records that name at least one of these models by its device identifier, newest first. Each recall usually covers specific models or lots, so check the details.
- Mar 16, 2023Open, Classified
JULIET Lateral Lumbar Ti-Life Plate, a component of the JULIET Ti Lateral Lumbar Cage, may disassemble during the preparation stage before implantation, or during surgery when removing the implant holder, which could cause surgical delay.
Z-1426-2023 · Root cause: Process change control · names 11 of these models · Recall details · FDA record ↗
Most reported JULIET Ti LL problems
Device problems
- Adverse Event Without Identified Device or Use Problem2
Patient problems
- Abdominal Pain1
- Hernia1
- Obstruction/Occlusion1
- Vertebral Fracture1
JULIET Ti LL models
13 models, most reported first. Each model has its own page with its reports, recalls and device details.
- JULIET ® Ti LL JLT-PL 02 08-SIntervertebral Fusion Device With Integrated Fixation, Lumbar1 recall0 reports
- JULIET ® Ti LL JLT-PL 02 10-SIntervertebral Fusion Device With Bone Graft, Lumbar1 recall0 reports
- JULIET ® Ti LL JLT-PL 02 12-SIntervertebral Fusion Device With Integrated Fixation, Lumbar1 recall0 reports
- JULIET ® Ti LL JLT-PL 02 14-SIntervertebral Fusion Device With Bone Graft, Lumbar1 recall0 reports
- JULIET ® Ti LL JLT-PL 02 16-SIntervertebral Fusion Device With Integrated Fixation, Lumbar1 recall0 reports
- JULIET ® Ti LL JLT-PL 04 08-SIntervertebral Fusion Device With Bone Graft, Lumbar1 recall0 reports
- JULIET ® Ti LL JLT-PL 04 10-SIntervertebral Fusion Device With Integrated Fixation, Lumbar1 recall0 reports
- JULIET ® Ti LL JLT-PL 04 12-SIntervertebral Fusion Device With Bone Graft, Lumbar1 recall0 reports
- JULIET ® Ti LL JLT-PL 04 14-SIntervertebral Fusion Device With Integrated Fixation, Lumbar1 recall0 reports
- JULIET ® Ti LL JLT-PL 04 16-SIntervertebral Fusion Device With Bone Graft, Lumbar1 recall0 reports
- JULIET ® Ti LL JLT-PL 04 18-SIntervertebral Fusion Device With Integrated Fixation, Lumbar1 recall0 reports
- JULIET ® Ti LL JLT-MX 50 14-SIntervertebral Fusion Device With Bone Graft, Lumbar1 report
- JULIET ® Ti LL JLT-MX 60 16-SIntervertebral Fusion Device With Integrated Fixation, Lumbar1 report
Recent JULIET Ti LL adverse event reports
The 2 most recent reports across all models, 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 ↗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 ↗
Other SpineArt SA products
All SpineArt SA devices →Sources and updates
- Models: FDA GUDID, file dated Oct 13, 2026. Models are grouped by the brand name the manufacturer registered.
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- 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.
How reports and recalls are matched · Editorial policy · Report an error on this page