JULIET ® Ti PO JUT-P6 24 11-SRecalls & reported problems
SpineArt SA · LUMBAR POSTERIOR Ti CAGE · Class 2 · Implant
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 07640178973466), received between Aug 28, 2023 and Aug 28, 2023 — classified as 1 injury.
The most frequently reported specific device problem is “Microbial Contamination of Device” (1 report).
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.
Most reported problems
Device problems
- Microbial Contamination of Device1
Patient problems
- Implant Pain1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryAug 28, 2023Microbial Contamination of Device; Microbial Contamination of Device
THE CUSTOMER COMPLAINT FORM REPORTS A POST-OPERATIVE INFECTION AND A REVISION SURGERY. THE PRIMO SURGERY WAS REALIZED ON (B)(6) 2022. THE PATIENT SUFFERED FROM PAIN SINCE (B)(6)2022. A POST-OPERATIVE INFECTION HAS BEEN DETECTED AND A REVISION SURGERY WAS REALIZED ON (B)(6) 2022 EXPLANTATION OF THE 2 CAGES (THE SCREWS AND THE SETSCREWS WERE NOT REMOVED) BECAUSE OF PSEUDARTHROSIS AND OSTEOLYSIS. ANTIBIOTIC TREATMENT UNTIL (B)(6) 2022. THE PATIENT IS FINE.
Patient problems: Implant Pain
MAUDE report 17630673 ↗
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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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