EIT LLIF cage LUI80849Recalls & reported problems
EIT Emerging Implant Technologies GmbH · EIT LLIF, H 8mm, 8°, 50/18 · Class 2 · Implant
- 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 04260557834725), received between Mar 5, 2026 and Mar 5, 2026 — 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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem1
Patient problems
- Paralysis1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryMar 5, 2026Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT THIS WAS AN OBLIQUE LATERAL INTERBODY FUSION(L3-L4) PERFORMED ON (B)(6) 2026. DURING THE SURGERY, THE CAGE WAS PLACED FURTHER BACK THAN USUAL, BUT THE WOUND WAS CLOSED BY THE SURGEON¿S DECISION. AFTER THE SURGERY, THE PARALYSIS ON THE PATIENT¿S LEG WAS CONFIRMED. THE REOPERATION TO REPLACE FURTHER FORWARD THAN PRIMARY SURGERY THE CAGE, THE OPERATION WAS COMPLETED SUCCESSFULLY WITH 120 MINUTES SURGICAL DELAY. THE PATIENT'S CONDITION AFTER THE SURGERY IS UNKNOWN.
Patient problems: Paralysis
MAUDE report 24519981 ↗
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- T-PAL 03.812.001Synthes GmbH · Intervertebral fusion device with bone graft, lumbar76 reports
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.