ANTHEM 2171.6526Recalls & reported problems
Globus Medical, Inc. · Non-Locking Screw, 2.5 X 26mm, SS · Class 2
All models of ANTHEM (27)
Data updated Oct 16, 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 00889095401998), received between Nov 20, 2025 and Nov 20, 2025 — classified as 1 malfunction.
The most frequently reported specific device problem is “Fracture” (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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Reports received per month
Most reported problems
Device problems
- Fracture1
Patient problems
- Foreign Body In Patient1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionNov 20, 2025Fracture; Fracture
IT WAS REPORTED THAT WHILE PLACING THE SCREWS DURING THE ORIF LEFT HUMERUS, IT WAS DISCOVERED THAT THREE 26MM NL SCREWS AND ONE 24MM NL SCREW BROKE. THE SURGEON ATTEMPTED TO RETRIEVE ALL PARTS OF THE SCREWS. IT WAS CONFIRMED BY SURGEON, REP, ADDITIONAL STAFF, AND X-RAY THAT PARTS OF THE FOUR SCREWS WERE UNABLE TO BE RETRIEVED AND THEREFORE LEFT IN THE PATIENT.
Patient problems: Foreign Body In Patient
MAUDE report 23605550 ↗
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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
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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