NA 04.613.514Recalls & reported problems
Synthes GmbH · 4.0MM TI CERV SELF-RETAIN SCR SLF-DRLG/VARIABLE ANGLE 14MM · Class 2 · Implant
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10705034737621), received between Oct 30, 2024 and Oct 30, 2024 — classified as 1 malfunction.
The most frequently reported specific device problem is “Mechanical Problem” (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 16, 2026.
Reports received per month
Most reported problems
Device problems
- Mechanical Problem1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionOct 30, 2024Mechanical Problem; Mechanical Problem
IT WAS REPORTED THAT THIS WAS A ACDF PERFORMED ON (B)(6) 2024. THE SURGEON HAD EXPERIENCE WITH CERVIC-SPINE-SCREW AND USED IT DURING SURGERY AS USUAL. HOWEVER, CERVIC-SPINE-SCREW IN QUESTION DID NOT WORK AS EXPECTED. THEREFORE, IT WAS REPLACED WITH A LONGER SIZE AND THE SURGERY WAS COMPLETED SUCCESSFULLY WITHOUT ANY SURGICAL DELAY. NO FURTHER INFORMATION IS AVAILABLE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20567838 ↗
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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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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