Veritas rTSA 1500-1030Recalls & reported problems
Restor3d, Inc. · Screw Baseplate, 30 mm · Class 2 · Implant
All models of Veritas rTSA (7)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 1
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00840097513225), received between Jul 10, 2026 and Jul 10, 2026 — classified as 1 malfunction.
1 FDA recall record name this device's identifier, 1 still open.
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
Recalls naming this device
- Jun 30, 2026Class IIOpen, Classified
Due to incorrect machining of peripheral screw hole resulting in potential for improper engagement of the peripheral screws.
Z-2987-2026 · Root cause: Device Design · Recall details · FDA record ↗
Most reported problems
Device problems
- No Apparent Adverse Event1
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.
MalfunctionJul 10, 2026No Apparent Adverse Event
THE SURGEON USED A COMPRESSION SCRWE WITH THE STANDARD VERITAS BASEPLATE. WHILE COMPLETING FINAL TORQUE, THE COMPRESSION SCREW PUSHED THROUGH THE BASEPLATE. THE SALES REPRESENTATIVE NOTED THAT THE WEEK PRIOR THERE WAS A BASEPLATE THAT HAS A COMPRESSION SCREW SEAT LOWER THAN EXPECTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25778977 ↗
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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 · each recall links to the FDA recall notice
- 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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