SYMPHONY 1020-24-002SRecalls & reported problems
Medos International Sàrl · SYMPHONY OCT SYSTEM CROSSCONNECTOR ROD TO ROD 26 to 32mm · Class 2 · Implant
All models of SYMPHONY (113)
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 10705034520209), received between May 13, 2022 and Jul 14, 2025 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Device-Device Incompatibility” (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 16, 2026.
Reports received per month
Most reported problems
Device problems
- Device-Device Incompatibility2
- 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.
MalfunctionJul 14, 2025Device-Device Incompatibility; Device-Device Incompatibility
IT WAS REPORTED THAT THIS WAS AN UNKNOWN SURGERY PERFORMED ON (B)(6) 2025. THE SURGERY WAS COMPLETED SUCCESSFULLY WITHOUT ANY SURGICAL DELAY. ON (B)(6) 2025, THE SALES REP WAS INFORMED BY A SURGEON THAT ON (B)(6) SURGERY, THE CROSS CONNECTOR IN QUESTION INTERFERED WITH THE SCREW HEAD AND COULD NOT BE PLACED. ANOTHER CROSS CONNECTOR WAS CUT AND USED AND THE SURGERY WAS COMPLETED WITHOUT PROBLEM. NO FURTHER INFORMATION IS AVAILABLE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22502413 ↗MalfunctionMay 13, 2022Device-Device Incompatibility; Material Deformation; Device-Device Incompatibility; Material Deformation
DEVICE REPORT FROM SYNTHES REPORTS AN EVENT IN JAPAN AS FOLLOWS: IT WAS REPORTED INTRAOPERATIVELY ON (B)(6) 2022 FOR A SPINE PCF (C3-5) PROCEDURE ON THAT THIS WAS A PCF (C3-5), A ROD WAS NOT ABLE TO BE DEPLOYED ON THE CONNECTOR. IT SEEMED THAT THE CONNECTOR¿S BASE AREA WHERE THE ROD WAS SUPPOSED TO BE PLACED MIGHT HAVE BEEN DEFORMED. AS A RESULT, THE SETSCREW BECAME IMMOVABLE. THE PROCEDURE WAS COMPLETED WITH REPLACEMENTS LESS THAN 30-MINUTE SURGICAL DELAY. CONCOMITANT DEVICE REPORTED: UNKNOWN RODS (PART# UNKNOWN; LOT# UNKNOWN; QUANTITY: 1). THIS IS REPORT 1 OF 1 FOR PC- (B)(4). THIS REPORT IS FOR CROSSCONNECTOR.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 14395930 ↗
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- 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
- EXPEDIUM VIPER 196789480Depuy Spine, LLC · APPLIANCE, FIXATION, SPINAL INTERLAMINAL72 reports
- NA 04.615.014Synthes GmbH · 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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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