FDA Adverse Event Injury Summary report: N

TRIOS CERVICAL MANAGEMENT BASE UNIT

MDR report key: 24745395 · Received March 31, 2026

Report

Report Number
2921578-2026-00007
Event Type
Injury
Date Received
March 31, 2026
Date of Event
March 5, 2026
Report Date
April 29, 2026
Manufacturer
MIZUHO ORTHOPEDIC SYSTEMS, INC.
Product Code
JEA
UDI-DI
00842430106101
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
US
Reporter Occupation
NURSE
Health Professional
Yes

Narratives

Additional Manufacturer Narrative · 0

THE LACERATIONS WERE CAUSED BY SKULL PINS THAT ARE NOT MANUFACTURED BY MIZUHO ORTHOPEDIC SYSTEMS, INC. (DBA- MIZUHO OSI). MAYFIELD SKULL PINS AND SKULL CLAMP (NON-MIZUHO OSI PRODUCTS) WERE ATTACHED TO MIZUHO OSI TRIOS CERVICAL MANAGEMENT BASE UNIT (CMBU) FOR THE INTENDED SURGICAL PROCEDURE WHICH IS SUSPECTED TO HAVE CONTRIBUTED TO THE REPORTED PATIENT INJURY. FURTHER INVESTIGATION OF THIS INCIDENT CONFIRMED THE PART NUMBER AND SERIAL NUMBER OF THE MIZUHO OSI PRODUCT THAT WAS SUSPECTED TO HAVE CONTRIBUTED TO THE PATIENT INJURY. THE ROOT CAUSE OF THIS INCIDENT IS PRIMARILY ATTRIBUTED TO USE ERROR. SPECIFICALLY, NO DOCUMENTED EVIDENCE WAS FOUND TO SUBSTANTIATE THAT HOSPITAL PERSONNEL WERE TRAINED ON EITHER THE THEORETICAL COMPONENTS (AS OUTLINED IN THE OWNER'S MANUAL) OR THE PRACTICAL OPERATIONAL ASPECTS OF THE MIZUHO OSI AND MAYFIELD DEVICES IN SCOPE. ADDITIONALLY, A FAILURE TO ADHERE TO ESTABLISHED BEST PRACTICES SET FORTH BY THE DEVICE MANUFACTURER WAS IDENTIFIED AS THE MAIN CAUSAL FACTOR. WHILE PATIENT STATURE MAY BE CONSIDERED A CONTRIBUTING FACTOR, CAUSATIVE PRECEDENCE IS ASSIGNED TO THE USE OF THE DEVICE BEYOND ITS INTENDED DESIGN LIFE AND THE FAILURE TO COMPLY WITH MANUFACTURER-DEFINED BEST PRACTICES FOR PATIENT SAFETY.

Additional Manufacturer Narrative · 0

THE LACERATIONS WERE CAUSED BY SKULL PINS THAT ARE NOT MANUFACTURED BY MIZUHO ORTHOPEDIC SYSTEMS, INC. (DBA- MIZUHO OSI). MAYFIELD SKULL PINS AND SKULL CLAMP (NON-MIZUHO OSI PRODUCTS) WERE ATTACHED TO MIZUHO OSI TRIOS CERVICAL MANAGEMENT BASE UNIT (CMBU) FOR THE INTENDED SURGICAL PROCEDURE WHICH IS SUSPECTED TO HAVE CONTRIBUTED TO THE REPORTED PATIENT INJURY.

Description of Event or Problem · 0

TRIOS SPINAL TABLE WITH CMBU (CERVICAL MANAGEMENT BASE UNIT) WAS UTILIZED FOR AN ANTERIOR-POSTERIOR FLIP PROCEDURE ON AN 80-YEAR-OLD PATIENT WEIGHING APPROXIMATELY 75-85 LBS. THE HOSPITAL PERSONNEL HAD NOT PERFORMED THIS TECHNIQUE IN APPROXIMATELY 10 YEARS. PRIOR TO THE PROCEDURE, THE INITIAL REPORTER RECOMMENDED RESCHEDULING TO ALLOW FOR IN-SERVICE TRAINING; THIS RECOMMENDATION WAS DECLINED BY THE ASSISTANT SURGEON. DURING SETUP, THE CMBU WAS ATTACHED WITH DIRECTION FROM THE INITIAL REPORTER. THE SURGEON TIGHTENED THE CONNECTION OF MAYFIELD SKULL CLAMP WITH CMBU DESPITE NOT BEING RECOMMENDED BY THE INITIAL REPORTER. THE INITIAL REPORTER INTERVENED A SECOND TIME TO CORRECT IMPROPER POSITIONING OF THE CHEST PLATE AND HIP/THIGH COMBINATION COMPONENTS BEFORE COMPRESSION WAS ATTEMPTED. DUE TO THE PATIENT'S SMALL FRAME, ADEQUATE COMPRESSION COULD NOT BE ACHIEVED. WHEN THE FLAT TOP WAS RAISED IN AN ATTEMPT TO COMPENSATE, THE MAYFIELD SKULL CLAMP AND CMBU WERE IN A LOCKED STATE, RESULTING IN DISPLACEMENT OF THE SKULL PINS POSTERIORLY AND CAUSING LACERATIONS TO THE PATIENT. THE PROCEDURE WAS HALTED. THE SPINAL TABLE WAS REMOVED, AND THE PATIENT WAS SAFELY TRANSFERRED TO A BED. THE TABLE TOP WAS CHANGED TO A SPINAL TOP, AND THE PATIENT REMAINING SKULL-CLAMPED WAS REPOSITIONED ONTO THE SPINAL TOP. LACERATIONS WERE STITCHED AND THE SURGICAL CASE WAS SUBSEQUENTLY CONTINUED. BOTH SURGEONS WERE SPOKEN TO FOLLOWING THE EVENT AND REPORTED THEY WERE DOING WELL.

Description of Event or Problem · 0

TRIOS SPINAL TABLE WITH CMBU (CERVICAL MANAGEMENT BASE UNIT) WAS UTILIZED FOR AN ANTERIOR-POSTERIOR FLIP PROCEDURE ON AN 80-YEAR-OLD PATIENT WEIGHING APPROXIMATELY 75-85 LBS. THE HOSPITAL PERSONNEL HAD NOT PERFORMED THIS TECHNIQUE IN APPROXIMATELY 10 YEARS. PRIOR TO THE PROCEDURE, THE INITIAL REPORTER RECOMMENDED RESCHEDULING TO ALLOW FOR IN-SERVICE TRAINING; THIS RECOMMENDATION WAS DECLINED BY THE ASSISTANT SURGEON. DURING SETUP, THE CMBU WAS ATTACHED WITH DIRECTION FROM THE INITIAL REPORTER. THE SURGEON TIGHTENED THE CONNECTION OF MAYFIELD SKULL CLAMP WITH CMBU DESPITE NOT BEING RECOMMENDED BY THE INITIAL REPORTER. THE INITIAL REPORTER INTERVENED A SECOND TIME TO CORRECT IMPROPER POSITIONING OF THE CHEST PLATE AND HIP/THIGH COMBINATION COMPONENTS BEFORE COMPRESSION WAS ATTEMPTED. DUE TO THE PATIENT'S SMALL FRAME, ADEQUATE COMPRESSION COULD NOT BE ACHIEVED. WHEN THE FLAT TOP WAS RAISED IN AN ATTEMPT TO COMPENSATE, THE MAYFIELD SKULL CLAMP AND CMBU WERE IN A LOCKED STATE, RESULTING IN DISPLACEMENT OF THE SKULL PINS POSTERIORLY AND CAUSING LACERATIONS TO THE PATIENT. THE PROCEDURE WAS HALTED. THE SPINAL TABLE WAS REMOVED, AND THE PATIENT WAS SAFELY TRANSFERRED TO A BED. THE TABLE TOP WAS CHANGED TO A SPINAL TOP, AND THE PATIENT REMAINING SKULL-CLAMPED WAS REPOSITIONED ONTO THE SPINAL TOP. LACERATIONS WERE STITCHED AND THE SURGICAL CASE WAS SUBSEQUENTLY CONTINUED. BOTH SURGEONS WERE SPOKEN TO FOLLOWING THE EVENT AND REPORTED THEY WERE DOING WELL.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
801293 TRIOS CERVICAL MANAGEMENT BASE UNIT SURGICAL PATIENT POSITIONER JEA MIZUHO ORTHOPEDIC SYSTEMS, INC. 5979-1 00842430106101

Patients

Seq Age Sex Outcome Treatment
1 80 YR Unknown Other