EXPEDIUM 279702700Recalls & reported problems
Depuy Spine, LLC · EXPEDIUM SPINE SYSTEM DOUBLE-LEAD TAP 7.0mm 30-70mm Plus or Minus 1.33 Percent · Class 1
All models of EXPEDIUM (29)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10705034198651), received between Oct 5, 2023 and Sep 8, 2025 — classified as 2 malfunctions.
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. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Reports received per month
Most reported problems
Device problems
- Break1
- Material Deformation1
Patient problems
- No Clinical Signs, Symptoms or Conditions2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 8, 2025Material Deformation; Material Deformation
IT WAS REPORTED THAT ON AN UNKNOWN DATE, PRODUCT WAS BENT AND DAMAGED. THERE WAS NO PATIENT INVOLVEMENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22992700 ↗MalfunctionOct 5, 2023Break; Break
IT WAS REPORTED THAT ON SEPTEMBER 16, 2023, THE FACILITY NOTIFIED OF INSTRUMENTS THAT HAD BEEN BROKEN OR DAMAGED. THERE WAS NO PATIENT INVOLVEMENT. ISSUES WERE DISCOVERED POSTOPERATIVELY. THIS REPORT INVOLVES ONE EXPEDIUM SPINE SYSTEM DOUBLE-LEAD TAP 7.0MM 30-70MM PLUS OR MINUS 1.33 PERCENT. THIS IS REPORT 2 OF 9 FOR (B)(4)
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17875183 ↗
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
- NA 03.424.126Synthes GmbH · TAP, BONE1 recall0 reports
- N/A 876-474Medtronic Sofamor Danek, Inc. · 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 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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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