EIT CIF cage CUI4070SRecalls & reported problems
EIT Emerging Implant Technologies GmbH · EIT CIF cage, H 7mm, 4°, S · Class 2 · Implant
All models of EIT CIF cage (6)
Data updated Oct 16, 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 04260557770306), received between Mar 28, 2025 and Mar 28, 2025 — 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 16, 2026.
Reports received per month
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem1
Patient problems
- Nonunion/Delayed-union Bone Fracture1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryMar 28, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT ON (B)(6) 2024, THE ORIGINAL OPERATION TOOK PLACE. THE PATIENT RETURNED TO OFFICE FOR ROUTINE FOLLOW-UP AS WELL AS REVIEW OF LUMBAR SPINE FOR SURGICAL INTERVENTION. THE SCREW BACK OUT WAS NOTICED ON FOLLOW-UP X-RAYS. SURGEON DETERMINED AT THE TIME HE WOULD REMOVE THE SCREW ON THE SAME DAY THE PATIENT WAS HAVING A POSTERIOR LUMBAR FUSION COMPLETED. REVISION WAS PERFORMED. CODA 48MM PLATE WAS ORIGINALLY IMPLANTED WITH 3.5X16 SCREWS IN C7. THERE WAS BILATERAL FLANGE BREAKAGE OVER C7 SCREWS. REMOVED C7 SCREWS. BOTH SCREWS WERE BROKEN AND TIPS OF SCREWS REMAINED IN THE VERTEBRAL BODY. UPON REVIEW OF THE CONSTRUCT, THE SURGEON DETERMINED THE PLATE WAS NOT REMAINING FLUSH WITH THE VERTEBRAL BODIES WHICH INDICATED POTENTIAL MOVEMENT AT THE ADJACENT LEVELS. HE MADE THE DECISION TO REMOVE THE PLATE AND REPLACE IT WITH SKYLINE TO AVOID ADDITIONAL SCREW/PLATE BREAKAGE OF THE EXISTING CODA PLATE. SURGEON MANUALLY ATTACHED REMOVAL TOOL TO CAGE AT EACH LEVEL AND DETERMINED THERE WAS NO CAGE LOOSENING AT C4/5, C5/C6. CAGE AT C6/C7 APPEARED TO SHOW SIGNS OF NONUNION PROMPTING SURGEON TO REMOVE THE 7MM 4* CONDUIT CAGE. A NEW CONDUIT 9MM 8* PACKED WITH VIVIGEN WAS PLACED IN THE C
Patient problems: Nonunion/Delayed-union Bone Fracture
MAUDE report 21719124 ↗
Other Intervertebral Fusion Device With Bone Graft, Cervical devices
- EIT CIF cage CUI8070SEIT Emerging Implant Technologies GmbH · Intervertebral Fusion Device With Bone Graft, Cervical1 recall4 reports
- ROI-C MC1005TLDR Spine Usa, Inc. · Intervertebral Fusion Device With Bone Graft, Cervical54 reports
- EIT CIF cage CUI8060LEIT Emerging Implant Technologies GmbH · Intervertebral Fusion Device With Bone Graft, Cervical1 recall1 report
- CONSTRUX - MINI PTC 37-5012SPOrthofix US LLC · Intervertebral fusion device with bone graft, cervical1 recall0 reports
- CONSTRUX - MINI Ti 37-6211SPOrthofix US LLC · Intervertebral fusion device with bone graft, cervical1 recall0 reports
- CONSTRUX - MINI Ti 37-7308SPOrthofix US LLC · Intervertebral fusion device with bone graft, cervical1 recall0 reports
- CONSTRUX - MINI Ti 37-9207SPOrthofix US LLC · Intervertebral fusion device with bone graft, cervical1 recall0 reports
- CONSTRUX - MINI Ti 37-6106SPOrthofix US LLC · Intervertebral fusion device with bone graft, cervical1 recall0 reports
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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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