XIA 3 48230055Recalls & reported problems
Stryker Corporation · MODULAR TAP · Class 1
Data updated Oct 13, 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 07613327264883), received between Sep 13, 2016 and Aug 10, 2017 — classified as 4 malfunctions.
The most frequently reported specific device problem is “Break” (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. How this data works · Data updated Oct 13, 2026.
Most reported problems
Device problems
- Break4
- Fracture4
- Material Integrity Problem3
- Loose or Intermittent Connection1
Patient problems
- No Known Impact Or Consequence To Patient4
- No Information1
Recent adverse event reports
The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.
MalfunctionAug 10, 2017Fracture; Material Integrity Problem; Break; Fracture; Material Integrity Problem
IT IS REPORTED THAT MODULAR TAP BROKE DURING SCREWING IN INTO THE VERTEBRAL BODY. REPLACEMENT WAS AVAILABLE.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 6786685 ↗MalfunctionApr 28, 2017Break; Fracture; Loose or Intermittent Connection; Material Integrity Problem; Fracture; Material Integrity Problem
IT WAS REPORTED THAT; NOTICED A BROKEN TAP AND LOOSE HINGED ROD HOLDER.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 6530470 ↗MalfunctionNov 15, 2016Fracture; Material Integrity Problem; Break; Fracture; Material Integrity Problem
IT WAS REPORTED THAT; 5.5 MM TAP BROKE DURING SURGERY.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 6104712 ↗MalfunctionSep 13, 2016Break; Fracture; Fracture
IT WAS REPORTED THAT THE TAP BROKE WHILE TAPPING PEDICLE.
Patient problems: No Information; No Known Impact Or Consequence To Patient
MAUDE report 5945556 ↗
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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 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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