inforMED
MalfunctionNOF

ITERO LUMINA SCANNING UNIT

Received Jun 25, 2025 · Event occurred Jun 10, 2025

Report 3009646999-2025-00430 · MDR key 22327742

Device

Generic name

System, Optical Impression, Computer Assisted Design And Manufacturing (cad/cam)

Model number

222100

Product problems

  • Insufficient Device Problem Information
  • Insufficient Device Problem Information

Patient

NA · Female

  • Burn(s)
  • Electric Shock
  • Burn(s)
  • Electric Shock

Narrative

Additional Manufacturer Narrative

THE CURRENT USER MANUAL CONTAINS THE FOLLOWING: "SCANNER PRECAUTIONS - AVOID TWISTING, KNOTTING, PULLING, AND STEPPING ON THE WAND CABLE AND THE POWER CABLE", "WARNING - DO NOT CONNECT THE SCANNER TO A MAIN SUPPLY WITHOUT PROTECTIVE GROUNDING, IN ORDER TO AVOID THE RISK OF ELECTRICAL SHOCK.". THIS EVENT IS BEING FILED AS AN MDR AS THE USER EXPERIENCED A MINOR INJURY ON HAND, REQUIRING MEDICAL CARE, AND THE ALIGN TECHNOLOGY, LTD MEDICAL DEVICE WAS BEING USED. INVESTIGATION OF THIS EVENT IS CURRENTLY ONGOING. A SUPPLEMENTAL REPORT WILL BE SUBMITTED WHEN ADDITIONAL INFORMATION BECOMES AVAILABLE.

Description of Event or Problem

THE COMPLAINANT REPORTED THAT AT THE MOMENT OF THE EVENT WHEN THE CHARGER WAS PLUGGED INTO THE POWER OUTLET IT BLEW UP, CAUSING A SKIN BURN IN THE HAND AND RECEIVED AN ELECTRIC SHOCK. THE USER REQUIRED A MEDICAL CHECK, AND WAS REVIEWED BY A CARDIOLOGIST, SURGEON AND OCCUPATIONAL MEDICINE DOCTOR AND IT IS UNKNOWN IF MEDICATIONS WERE PRESCRIBED TO ALLEVIATE THE REPORTED SYMPTOMS.

Additional Manufacturer Narrative

AN INVESTIGATION INTO THE DEVICE INVOLVED IN THE REPORTED EVENT HAS BEEN COMPLETED. FINDINGS INDICATE THAT THE INCIDENT IS ASSOCIATED WITH A PREVIOUSLY IDENTIFIED ISSUE, WHICH HAS ALREADY BEEN ADDRESSED THROUGH DESIGN MODIFICATIONS IN THE ACCESSORY COMPONENTS. THE COMPONENT IMPLICATED IN THIS EVENT BELONGS TO AN EARLIER DESIGN ITERATION. THE INVESTIGATION ALSO REVEALED A MISCOMMUNICATION BETWEEN THE USER AND THE SUPPORT AGENT, RESULTING IN THE DISPATCH OF AN INCORRECT COMPONENT. FURTHERMORE, BASED ON THE USER INTERVIEW, IT WAS DETERMINED THAT THE USER DID NOT FOLLOW THE INSTRUCTIONS OUTLINED IN THE USER MANUAL REGARDING THE CORRECT SEQUENCE FOR CONNECTING THE COMPONENTS. THE DEVICE INVOLVED IN THE EVENTS IS A LUMINA DEVICE THAT HAS BEEN UPGRADED FROM A 5D DEVICE. THE 5D DEVICE HAS BEEN ACTIVE SINCE MAY-2021, THUS THE INVOLVED COMPETENT IS ABOUT 4 YEARS OLD. THIS DEVIATION FROM THE RECOMMENDED PROCEDURE CONTRIBUTED TO SUBSEQUENT HARM TO THE USER. SECTION H6 CODES UPDATED TO REFLECT THE FINAL INVESTIGATION.