MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,user f report with the FDA on 2020-02-27 for ADVANCED CONTROL I-BASE, DC 5803 manufactured by Mizuho Orthopedic Systems, Inc..
[183889738]
It was reported that the table attempted to be moved/tilted in the operating room (or) and the patient almost fell down - status of the patient unknown.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 2921578-2020-00010 |
MDR Report Key | 9763213 |
Report Source | COMPANY REPRESENTATIVE,USER F |
Date Received | 2020-02-27 |
Date of Report | 2020-02-27 |
Date Mfgr Received | 2020-02-24 |
Device Manufacturer Date | 2015-08-31 |
Date Added to Maude | 2020-02-27 |
Event Key | 0 |
Report Source Code | Manufacturer report |
Manufacturer Link | Y |
Number of Patients in Event | 0 |
Adverse Event Flag | 3 |
Product Problem Flag | 3 |
Reprocessed and Reused Flag | 3 |
Reporter Occupation | BIOMEDICAL ENGINEER |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 3 |
Event Location | 3 |
Manufacturer Contact | ANNE LEBLANC |
Manufacturer Street | 30031 AHERN AVENUE |
Manufacturer City | UNION CITY, CA |
Manufacturer Country | US |
Manufacturer Phone | 4291500233 |
Manufacturer G1 | MIZUHO ORTHOPEDIC SYSTEMS, INC. |
Manufacturer Street | 30031 AHERN AVENUE |
Manufacturer City | UNION CITY, CA |
Manufacturer Country | US |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | ADVANCED CONTROL I-BASE, DC |
Generic Name | SURGICAL OPERATING TABLE |
Product Code | JEA |
Date Received | 2020-02-27 |
Model Number | 5803 |
Catalog Number | 5803 |
Operator | HEALTH PROFESSIONAL |
Device Availability | Y |
Device Eval'ed by Mfgr | N |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | MIZUHO ORTHOPEDIC SYSTEMS, INC. |
Manufacturer Address | 30031 AHERN AVENUE UNION CITY, CA US |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2020-02-27 |