Invictus 19807-30Recalls & reported problems
Alphatec Spine, Inc. · Tap, Cervical, 3.0mm · Class 1
Data updated Oct 13, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 8
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 8 adverse event reports that list this exact device (DI 00190376301518), received between Oct 14, 2024 and Jun 29, 2026 — classified as 8 malfunctions.
The most frequently reported specific device problem is “Break” (8 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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Break8
- Material Separation3
Patient problems
- No Clinical Signs, Symptoms or Conditions8
Recent adverse event reports
The 8 most recent of 8 reports, in the reporter's own words as published by the FDA.
MalfunctionJun 29, 2026Break
THE TIP OF THE TAP BROKE OFF INTO BONE DURING INSERTION. THE BROKEN FRAGMENT WAS RETRIEVED WITHOUT INCIDENT, AND THE INSTRUMENT WAS DISCARDED AT THE HOSPITAL.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25659109 ↗MalfunctionMay 11, 2026Break
IT WAS REPORTED THAT THE TAP BROKE DURING SCREW PREPARATION. THE TIP WAS RETRIEVED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25137139 ↗MalfunctionMar 19, 2026Break; Material Separation
IT WAS REPORTED THAT THE TAP BROKE AT THE C2 LEVEL DURING A SPINAL PROCEDURE. THE BROKEN PIECES WERE RETRIEVED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24642904 ↗MalfunctionSep 11, 2025Break; Material Separation; Break; Material Separation
IT WAS REPORTED THAT THE TIP OF THE DRIVER HAS BROKEN OFF.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23029955 ↗MalfunctionJun 9, 2025Break; Material Separation; Break; Material Separation
IT WAS REPORTED THAT THE TIP OF THE TAP BROKE OFF DURING A CASE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22169063 ↗MalfunctionJan 10, 2025Break; Break
IT WAS REPORTED THAT THE TAP BROKE DURING SURGERY. NO PIECES WERE LEFT IN THE PATIENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21125525 ↗MalfunctionOct 14, 2024Break; Break
WHEN THE SURGEON WAS USING THE TAP, THE TIP BROKE OFF IN THE BONE. THE SURGEON WAS ABLE TO RETRIEVE THE TIP. NO FURTHER COMPLICATIONS WERE REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20441054 ↗MalfunctionOct 14, 2024Break; Break
IT WAS REPORTED THAT THE TAP BROKE DURING A PROCEDURE. THE BROKEN PIECE WAS RETRIEVED. NO FURTHER COMPLICATIONS WERE REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20440998 ↗
Other TAP, BONE devices
- NA 311.43Synthes GmbH · TAP, BONE176 reports
- NA 311.01Synthes GmbH · TAP, BONE106 reports
- NA 311.431Synthes GmbH · TAP, BONE70 reports
- NA 03.424.124Synthes GmbH · TAP, BONE1 recall7 reports
- N/A 876-474Medtronic Sofamor Danek, Inc. · TAP, BONE1 recall0 reports
- NA 03.424.126Synthes GmbH · TAP, BONE1 recall0 reports
- A.L.P.S.® 8241-50-170Biomet Orthopedics, LLC · TAP, BONE1 recall0 reports
- NA 311.44Synthes GmbH · TAP, BONE41 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 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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