EXPEDIUM 279792114Recalls & reported problems
Medos International Sàrl · EXPEDIUM SPINE SYSTEM SCREW CASE 5.5 · Class 1
All models of EXPEDIUM (291)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 10705034459820), received between Jul 24, 2023 and Aug 18, 2023 — classified as 3 malfunctions.
The most frequently reported specific device problem is “Material Twisted/Bent” (3 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 16, 2026.
Most reported problems
Device problems
- Material Twisted/Bent3
Patient problems
- No Clinical Signs, Symptoms or Conditions3
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionAug 18, 2023Material Twisted/Bent; Material Twisted/Bent
IT WAS REPORTED THAT ON AN UNKNOWN DATE, THE INSTRUMENTS WERE FOUND TO BE WORN DOWN DURING INSPECTION OF EQUIPMENT. THIS REPORT INVOLVES ONE EXPEDIUM SPINE SYSTEM SCREW CASE 5.5. THIS IS REPORT 1 OF 1 FOR (B)(4) .
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17572989 ↗MalfunctionJul 24, 2023Material Twisted/Bent; Material Twisted/Bent
IT WAS REPORTED THAT DURING POSTOPERATIVE INSPECTION OF THE EQUIPMENT ON AN UNKNOWN DATE, INSTRUMENTS WERE FOUND TO BE WORN DOWN AND NEEDED REPLACEMENT. THIS REPORT INVOLVES ONE EXPEDIUM SPINE SYSTEM SCREW CASE 5.5. THIS IS REPORT 1 OF 2 FOR (B)(4).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17377262 ↗MalfunctionJul 24, 2023Material Twisted/Bent; Material Twisted/Bent
HOLD FOR KR 7/24 IT WAS REPORTED THAT DURING POSTOPERATIVE INSPECTION OF THE EQUIPMENT ON AN UNKNOWN DATE, INSTRUMENTS WERE FOUND TO BE WORN DOWN AND NEEDED REPLACEMENT. THIS REPORT INVOLVES ONE EXPEDIUM SPINE SYSTEM SCREW CASE 5.5. THIS IS REPORT 2 OF 2 FOR (B)(4).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17377255 ↗
Other TRAY, SURGICAL, INSTRUMENT devices
- PINNACLE 2220-00-100Depuy (Ireland) · TRAY, SURGICAL, INSTRUMENT74 reports
- ACTIS 2010-04-200Depuy (Ireland) · TRAY, SURGICAL, INSTRUMENT66 reports
- ATTUNE 2545-01-703Depuy (Ireland) · TRAY, SURGICAL, INSTRUMENT62 reports
- ATTUNE 2545-01-704Depuy (Ireland) · TRAY, SURGICAL, INSTRUMENT57 reports
- n.a. 39501XKarl Storz GmbH & Co. KG · TRAY, SURGICAL, INSTRUMENT1 recall0 reports
- Medical Action Industries 6810Medical Action Industries Inc. · TRAY, SURGICAL, INSTRUMENT1 recall0 reports
- n.a. 39501BECKarl Storz GmbH & Co. KG · TRAY, SURGICAL, INSTRUMENT1 recall0 reports
- n.a. 39501XKKarl Storz GmbH & Co. KG · TRAY, SURGICAL, INSTRUMENT1 recall0 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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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