XIA 3 48236030Recalls & reported problems
Stryker Corporation · 30-35 mm MULTI AXIAL CROSS CONNECTOR · Class 2 · Implant
Data updated Oct 13, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 04546540560858), received between Jul 18, 2017 and Jul 18, 2017 — classified as 1 malfunction.
The most frequently reported specific device problem is “Break” (1 report).
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
- Break1
- Mechanical Problem1
Patient problems
- No Known Impact Or Consequence To Patient1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionJul 18, 2017Mechanical Problem; Break; Mechanical Problem
IT WAS REPORTED THAT; UPON GOING TO USE SEVERAL CROSS LINKS ON A LONG CONSTRUCT IT BECAME EVIDENT THAT SEVERAL OF THE SET SCREWS HAD BECOME DETHREADED FROM THE CROSS LINKS ITSELF. TYPICALLY WE CAN THREAD THESE BACK IN, WEAVER WITH THIS PARTICULAR BATCH, IT APPEARED AS THOUGHT ALL WERE "DAMAGED" OR OTHERWISE AFFECTED TO THE POINT WHERE WE COULD NO LONGER GET THE SET SCREW BACK INTO PLACE.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 6723512 ↗
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- LineSider LS-N6SA7550Integrity Implants Inc. · Thoracolumbosacral Pedicle Screw System2 recalls1 report
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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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