MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,foreig report with the FDA on 2020-03-03 for SELENIA MAMMOGRAPHY SYSTEM SEL-00002 manufactured by Hologic, Inc.
[182319498]
As of today the investigation is still in process and a follow up will be filed as needed.
Patient Sequence No: 1, Text Type: N, H10
[182319499]
It was reported that the c-arm is not parallel with the gantry and metal shavings are seen on the rotation collar. No injury reported. A field engineer was dispatched to the site.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 1220984-2020-00035 |
MDR Report Key | 9781750 |
Report Source | COMPANY REPRESENTATIVE,FOREIG |
Date Received | 2020-03-03 |
Date of Report | 2020-02-03 |
Date of Event | 2020-02-03 |
Date Mfgr Received | 2020-02-03 |
Device Manufacturer Date | 2007-03-01 |
Date Added to Maude | 2020-03-03 |
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 |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 3 |
Event Location | 3 |
Manufacturer Contact | KRISTIN FORNIERI |
Manufacturer Street | 36 & 37 APPLE RIDGE ROAD |
Manufacturer City | DANBURY, CT |
Manufacturer Country | US |
Manufacturer Phone | 7318491 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | SELENIA MAMMOGRAPHY SYSTEM |
Generic Name | FULL FIELD DIGITAL MAMMOGRAPHY SYSTEM |
Product Code | MUE |
Date Received | 2020-03-03 |
Model Number | SEL-00002 |
Catalog Number | SEL-00002 |
Operator | HEALTH PROFESSIONAL |
Device Availability | * |
Device Eval'ed by Mfgr | * |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | HOLOGIC, INC |
Manufacturer Address | 36 & 37 APPLE RIDGE ROAD DANBURY, CT US |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2020-03-03 |