Tapered Screw-Vent® Implant System 30AT424Recalls & reported problems
ZimVie US Corp LLC · Class 2 · Implant
All models of Tapered Screw-Vent Implant System (28)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 4
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 00889024013599), received between Jan 24, 2023 and Jan 27, 2023 — classified as 4 malfunctions.
The most frequently reported specific device problem is “Unintended Movement” (4 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
- Unintended Movement4
Patient problems
- No Clinical Signs, Symptoms or Conditions4
Recent adverse event reports
The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.
MalfunctionJan 27, 2023Unintended Movement; Unintended Movement
UPON FOLLOW UP, THE DISTRIBUTOR CONFIRMED THAT THE IMPLANTS WERE NOT REMOVED. ONLY THE SCREWS WERE REMOVED AND CHANGED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16259429 ↗MalfunctionJan 27, 2023Unintended Movement; Unintended Movement
UPON FOLLOW UP, THE DISTRIBUTOR CONFIRMED THAT THE IMPLANTS WERE NOT REMOVED. ONLY THE SCREWS WERE REMOVED AND CHANGED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16258074 ↗MalfunctionJan 24, 2023Unintended Movement; Unintended Movement
IT WAS REPORTED THAT THE IMPLANT WAS NOT REMOVED. ONLY SCREW REMOVED AND CHANGED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16233999 ↗MalfunctionJan 24, 2023Unintended Movement; Unintended Movement
IT WAS REPORTED THAT THE IMPLANT WAS NOT REMOVED. ONLY SCREW REMOVED AND CHANGED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16233995 ↗
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- Esthetic Abutment 36669Nobel Biocare AB · ABUTMENT, IMPLANT, DENTAL, ENDOSSEOUS1 recall2 reports
- CERTAIN® BELLATEK® IEDAT5ZimVie US Corp LLC · ABUTMENT, IMPLANT, DENTAL, ENDOSSEOUS1 recall1 report
- Custom Abutments Final AbutmentsInstitut Straumann AG · Abutment, implant, dental, endosseous1 recall0 reports
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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