UNK_REMOTION IMPLANT
Received Jan 21, 2026 · Event occurred Aug 6, 2024
Report 0008031020-2026-00076 · MDR key 24127436
Device
Generic name
Prosthesis, Wrist, 3 Part Metal-plastic-metal Articulation, Semi-constrained
Manufacturer
Stryker GmbhCatalog number
UNK_SEL
Lot number
UNKNOWN
Product problems
- Adverse Event Without Identified Device or Use Problem
Patient
NA · Unknown
- Loss of Range of Motion
Narrative
Description of Event or Problem
THE MANUFACTURER BECAME AWARE OF A LITERATURE PUBLISHED BY THE DEPARTMENT OF ORTHOPAEDICS AND TRAUMATOLOGY, PRINCE OF WALES HOSPITAL, SHATIN, HONG KONG. THE TITLE OF THIS REPORT IS COMPLICATIONS FOLLOWING TOTAL WRIST REPLACEMENT: A SINGLE-CENTER RETROSPECTIVE REVIEW, PUBLISHED ON 6 AUGUST 2024, WHICH IS ASSOCIATED WITH THE STRYKER REMOTION IMPLANT SYSTEM. THE ARTICLE CAN BE FOUND ON DOI: 10.1177/22104917241280976. DURING THE REVIEW OF THE LITERATURE, IT WAS NOT POSSIBLE TO ESTABLISH A SPECIFIC DEVICE DETAIL, PATIENT INFORMATION, AND AT THIS TIME NO ADDITIONAL DEVICE INFORMATION IS AVAILABLE. IT WAS REPORTED THAT: TWO PATIENTS HAD STIFFNESS WITHOUT NEED OF MUA (MANIPULATION UNDER ANESTHESIA). THIS IS 1 OF 2.
Additional Manufacturer Narrative
THIS COMPLAINT HAS BEEN GENERATED BASED ON FINDINGS IDENTIFIED DURING POST MARKET SURVEILLANCE LITERATURE. THE ARTICLE CAN BE FOUND AT DOI: 10.1177/22104917241280976. THE REPORTED EVENT COULD NOT BE CONFIRMED SINCE THE DEVICE WAS NOT RETURNED FOR EVALUATION AND NO OTHER ADDITIONAL INFORMATION WAS RECEIVED FROM THE AUTHOR. MORE DETAILED INFORMATION ABOUT THE PATIENT'S MEDICAL HISTORY, THE EVENT DETAILS AND THE INVOLVED DEVICE(S) MUST BE AVAILABLE TO DETERMINE THE ROOT CAUSE. IF ANY ADDITIONAL INFORMATION BECOMES AVAILABLE, THE INVESTIGATION WILL BE REOPENED AND RE-EVALUATED ACCORDINGLY.