4WEB Medical PSTS-SM0608-26-SPRecalls & reported problems
4web Medical · Class 2 · Implant
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- 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 00812998022502), received between Mar 8, 2019 and Mar 8, 2019 — 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. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Most reported problems
Device problems
- Migration2
Patient problems
- No Known Impact Or Consequence To Patient2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryMar 8, 2019Migration; Migration
IT WAS REPORTED THAT DURING THE PATIENT'S 6-WEEK FOLLOW-UP IT WAS FOUND THAT THE IMPLANT MIGRATED POSTERIORLY. THE COMPANY WAS NOTIFIED THAT THE PATIENT REQUIRED A REVISION SURGERY. NO COMPLICATIONS WERE REPORTED TO THE MANUFACTURER. THE PATIENT IS DOING WELL POST-OPERATIVELY. IT IS UNKNOWN WHICH DEVICE IS RELATED TO THE REPORTED INCIDENT. THEREFORE, BOTH DEVICES ARE BEING REPORTED. (DEVICE 2 OF 2).
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 8404425 ↗InjuryMar 8, 2019Migration; Migration
IT WAS REPORTED THAT DURING THE PATIENT'S 6-WEEK FOLLOW-UP IT WAS FOUND THAT THE IMPLANT MIGRATED POSTERIORLY. THE COMPANY WAS NOTIFIED THAT THE PATIENT REQUIRED A REVISION SURGERY. NO COMPLICATIONS WERE REPORTED TO THE MANUFACTURER. THE PATIENT IS DOING WELL POST-OPERATIVELY. IT IS UNKNOWN WHICH DEVICE IS RELATED TO THE REPORTED INCIDENT. THEREFORE, BOTH DEVICES ARE BEING REPORTED. (DEVICE 1 OF 2).
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 8404419 ↗
Other Intervertebral Fusion Device With Bone Graft, Lumbar devices
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- EIT TLIF Inserter TFT30101EIT Emerging Implant Technologies GmbH · Intervertebral Fusion Device With Bone Graft, Lumbar88 reports
- T-PAL 03.812.001Synthes GmbH · Intervertebral fusion device with bone graft, lumbar76 reports
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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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