EXPEDIUM VERSE 2997-04-306Recalls & reported problems
Medos International Sàrl · EXPEDIUM VERSE ADVANCE REDUCER · Class 1
All models of EXPEDIUM VERSE (90)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 6
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 6 adverse event reports that list this exact device (DI 10705034532905), received between Mar 22, 2021 and Mar 22, 2021 — classified as 6 malfunctions.
The most frequently reported specific device problem is “Device-Device Incompatibility” (6 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
- Device-Device Incompatibility6
- No Apparent Adverse Event3
Patient problems
- No Clinical Signs, Symptoms or Conditions6
Recent adverse event reports
The 6 most recent of 6 reports, in the reporter's own words as published by the FDA.
MalfunctionMar 22, 2021Device-Device Incompatibility; No Apparent Adverse Event; Device-Device Incompatibility; No Apparent Adverse Event
THESE PRODUCTS WERE NOT USED IN SURGERY, THEY WERE DISCOVERED DURING AN INSPECTION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 11547539 ↗MalfunctionMar 22, 2021Device-Device Incompatibility; No Apparent Adverse Event; Device-Device Incompatibility; No Apparent Adverse Event
THESE PRODUCTS WERE NOT USED IN SURGERY. THEY WERE DISCOVERED, DURING AN INSPECTION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 11547527 ↗MalfunctionMar 22, 2021Device-Device Incompatibility; No Apparent Adverse Event; Device-Device Incompatibility; No Apparent Adverse Event
THESE PRODUCTS WERE NOT USED IN SURGERY, THEY WERE DISCOVERED DURING AN INSPECTION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 11547468 ↗MalfunctionMar 22, 2021Device-Device Incompatibility; Device-Device Incompatibility
THESE PRODUCTS WERE NOT USED IN SURGERY, THEY WERE DISCOVERED DURING AN INSPECTION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 11547462 ↗MalfunctionMar 22, 2021Device-Device Incompatibility; Device-Device Incompatibility
THESE PRODUCTS WERE NOT USED IN SURGERY, THEY WERE DISCOVERED DURING AN INSPECTION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 11547443 ↗MalfunctionMar 22, 2021Device-Device Incompatibility; Device-Device Incompatibility
THESE PRODUCTS WERE NOT USED IN SURGERY, THEY WERE DISCOVERED DURING AN INSPECTION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 11547272 ↗
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- NA 03.010.523Synthes GmbH · ORTHOPEDIC MANUAL SURGICAL INSTRUMENT1,208 reports
- EXPRESSEW 214141Medos International Sàrl · ORTHOPEDIC MANUAL SURGICAL INSTRUMENT1,166 reports
- N/A 9560524Medtronic Sofamor Danek, Inc. · ORTHOPEDIC MANUAL SURGICAL INSTRUMENT866 reports
- INHANCE 6500-11-104Depuy (Ireland) · Orthopedic manual surgical instrument831 reports
- INHANCE 6500-11-102Depuy (Ireland) · Orthopedic manual surgical instrument567 reports
- R3 71364450Smith & Nephew, Inc. · ORTHOPEDIC MANUAL SURGICAL INSTRUMENT520 reports
- N/A 9561524Medtronic Sofamor Danek, Inc. · ORTHOPEDIC MANUAL SURGICAL INSTRUMENT494 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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