EXPEDIUM 179762381Recalls & reported problems
Medos International Sàrl · EXPEDIUM SPINE SYSTEM PRE-CONTOURED ROD, MEDIUM diameter 5.5mm · Class 2 · Implant
All models of EXPEDIUM (291)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10705034562599), received between Feb 14, 2024 and Feb 15, 2024 — classified as 2 injuries.
The most frequently reported specific device problem is “Break” (2 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. 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
- Break2
Patient problems
- Pain2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryFeb 15, 2024Break; Break
IT WAS REPORTED THE PATIENT HAD A SPINE CONSTRUCT IMPLANTED (B)(6) 2023 FROM T10 TO PELVIS. THE PATIENT WAS IMPLANTED WITH 2 EXPEDIUM RODS, AN UNKNOWN NUMBER VIPER AND EXPEDIUM SCREWS, AND TWO PELVIC SCREWS. PATIENT WAS EXPERIENCING PAIN AND HAD A FOLLOW UP (B)(6)2023. DURING THE FOLLOW UP IMAGES IDENTIFIED 2 BROKEN RODS AND AN UNKNOWN NUMBER OF MIGRATED SCREWS. THE PATIENT WILL BE HAVING A REVISION SURGERY ON (B)(6) 2024. THIS REPORT IS FOR ONE (1) UNK - RODS: EXPEDIUM THIS IS REPORT 1 OF 6 FOR COMPLAINT (B)(4).
Patient problems: Pain
MAUDE report 18711131 ↗InjuryFeb 14, 2024Break; Break
IT WAS REPORTED THE PATIENT HAD A SPINE CONSTRUCT IMPLANTED (B)(6) 2023 FROM T10 TO PELVIS. THE PATIENT WAS IMPLANTED WITH 2 EXPEDIUM RODS, AN UNKNOWN NUMBER VIPER AND EXPEDIUM SCREWS, AND TWO PELVIC SCREWS. PATIENT WAS EXPERIENCING PAIN AND HAD A FOLLOW UP (B)(6) 2023. DURING THE FOLLOW UP IMAGES IDENTIFIED 2 BROKEN RODS AND AN UNKNOWN NUMBER OF MIGRATED SCREWS. THE PATIENT WILL BE HAVING A REVISION SURGERY ON (B)(6) 2024. THIS REPORT IS FOR ONE (1) UNK - RODS: EXPEDIUM THIS IS REPORT 4 OF 6 FOR COMPLAINT (B)(4).
Patient problems: Pain
MAUDE report 18703321 ↗
Other APPLIANCE, FIXATION, SPINAL INTERLAMINAL devices
- EXPEDIUM 179702000Medos International Sàrl · APPLIANCE, FIXATION, SPINAL INTERLAMINAL439 reports
- EXPEDIUM VERSE 199721001Medos International Sàrl · APPLIANCE, FIXATION, SPINAL INTERLAMINAL227 reports
- XIA 3 48230000Stryker Corporation · APPLIANCE, FIXATION, SPINAL INTERLAMINAL193 reports
- VIPER 186715000Medos International Sàrl · APPLIANCE, FIXATION, SPINAL INTERLAMINAL1 death167 reports
- NA 04.614.014Synthes GmbH · APPLIANCE, FIXATION, SPINAL INTERLAMINAL80 reports
- NA 04.615.014Synthes GmbH · APPLIANCE, FIXATION, SPINAL INTERLAMINAL72 reports
- EXPEDIUM VIPER 196789480Depuy Spine, LLC · APPLIANCE, FIXATION, SPINAL INTERLAMINAL72 reports
- Arsenal Deformity Spinal Fixation System 47127Alphatec Spine, Inc. · APPLIANCE, FIXATION, SPINAL INTERLAMINAL66 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.
How reports and recalls are matched · Editorial policy · Report an error on this page