EIT PLIF cage PUI40902Recalls & reported problems
EIT Emerging Implant Technologies GmbH · EIT PLIF, H 9mm, 4°, 22/9 · Class 2 · Implant
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 04260557778401), received between Mar 5, 2026 and Mar 5, 2026 — classified as 2 injuries.
The most frequently reported specific device problem is “Migration” (2 reports).
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
- Migration2
Patient problems
- Insufficient Information2
- No Clinical Signs, Symptoms or Conditions2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryMar 5, 2026Migration
ADDITIONAL INFORMATION WAS RECEIVED AND STATES THAT: THERE WAS A PROBLEM WITH THE SCREW TRAJECTORY, SO ONE OF THE PRODUCTS WAS REMOVED.
Patient problems: Insufficient Information; No Clinical Signs, Symptoms or Conditions
MAUDE report 24519709 ↗InjuryMar 5, 2026Migration
ADDITIONAL INFORMATION WAS RECEIVED AND STATES THAT: THERE WAS A PROBLEM WITH THE SCREW TRAJECTORY, SO ONE OF THE PRODUCTS WAS REMOVED.
Patient problems: Insufficient Information; No Clinical Signs, Symptoms or Conditions
MAUDE report 24519607 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.