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4WEB Medical CSTS-MD0708Recalls & reported problems

4web Medical · 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 00812998020126), received between Apr 19, 2023 and Apr 19, 2023 — classified as 1 injury.

The most frequently reported specific device problem is “Insufficient Device Problem Information” (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

  • Adverse Event Without Identified Device or Use Problem1
  • Insufficient Device Problem Information1

Patient problems

  • Insufficient Information1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • InjuryApr 19, 2023Adverse Event Without Identified Device or Use Problem; Insufficient Device Problem Information; Adverse Event Without Identified Device or Use Problem; Insufficient Device Problem Information

    TWO (2) NON-STERILE CERVICAL SPINE IMPLANTS WERE RETURNED TO THE MANUFACTURER. UPON INSPECTION, IT WAS IDENTIFIED THAT THE DEVICES WERE EXPLANTED. NO INFORMATION WAS AVAILABLE ON THE EXPLANTATION. IT IS POSSIBLE THAT A REVISION SURGERY MAY HAVE BEEN PERFORMED, HOWEVER, NO CONFIRMATION WAS RECEIVED. (DEVICE 2 OF 2).

    Patient problems: Insufficient Information

    MAUDE report 16772855 ↗

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Sources and updates

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