4WEB Medical CSTS2-MD0708-SPRecalls & 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 00810074758383), received between Feb 24, 2026 and Feb 24, 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. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Reports received per month
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem1
Patient problems
- Fall1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryFeb 24, 2026Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED TO 4WEB MEDICAL THAT A 4WEB CERVICAL CAGE, PLATE, AND SCREWS WERE EXPLANTED FOLLOWING A FALL THAT COMPROMISED THE CONSTRUCT. THE REVISION SURGERY WAS PERFORMED ON (B)(6) 2026, LESS THAN ONE MONTH AFTER THE INITIAL SURGERY. NO ISSUES OR COMPLICATIONS WERE REPORTED DURING THE REVISION PROCEDURE. DEVICE 1 OF 3.
Patient problems: Fall
MAUDE report 24438626 ↗
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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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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