CONDUIT 187210210Recalls & reported problems
Medos International Sàrl · CONDUIT Lateral System Switch Plate, One-Hole, Type A, Small · Class 2 · Implant
All models of CONDUIT (27)
Data updated Oct 16, 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 10705034574554), received between Apr 12, 2023 and Jun 15, 2023 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Device Damaged Prior to Use” (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.
Most reported problems
Device problems
- Device Damaged Prior to Use1
- Device-Device Incompatibility1
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.
MalfunctionJun 15, 2023Device Damaged Prior to Use; Device Damaged Prior to Use
IT WAS REPORTED THAT ON MARCH 16, 2023, A DAMAGED SWITCH PLATE WAS RECEIVED VIA MAIL AT THE DEPUY RAYNHAM FACILITY FROM A REP. NO FURTHER DETAILS WERE PROVIDED. IT IS UNKNOWN WHEN THE ISSUE WAS DISCOVERED. IT IS UNKNOWN IF THERE WERE PATIENT AND PROCEDURE INVOLVEMENT. DURING MANUFACTURER'S INVESTIGATION OF THE RETURNED DEVICE IT WAS IDENTIFIED THAT THE SWITCH PLATE, 1H A, SMALL HAD THE CONDUIT LATERAL SWITCH PLATE, LOCK SHAFT UNATTACHED AND THE CONDUIT LATERAL SWITCH PLATE, LOCK PIN UNATTACHED WITH THE TIP BROKEN OFF. THIS REPORT IS FOR ONE (1) SWITCH PLATE, 1H A, SMALL. THIS IS REPORT 1 OF 1 FOR COMPLAINT (B)(4).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17132942 ↗MalfunctionApr 12, 2023Device-Device Incompatibility; Device-Device Incompatibility
IT WAS REPORTED THAT ON MARCH 8, 2023, THE PLATE WOULDN¿T LOCK TO CAGE. NO PATIENT ISSUES. THIS REPORT IS FOR ONE (1) SWITCH PLATE, 1H A, SMALL. THIS IS REPORT 1 OF 2 FOR (B)(4).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16722739 ↗
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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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