MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,health report with the FDA on 2020-03-09 for NOVASURE IMPEDANCE CONTROLLED EA SYSTEM NS2007 manufactured by Hologic, Inc.
[182686728]
The device is not being returned therefore, a failure analysis of the complaint device cannot be completed. If additional relevant information is received or device evaluation completed, a supplemental medwatch will be filed. Device history record (dhr) review was conducted for the reported identification number. The lot was released meeting all qa specifications.
Patient Sequence No: 1, Text Type: N, H10
[182686729]
It was reported that the patient underwent a successful endometrial ablation on (b)(6) 2020. It was reported that the patient was doing well post-ablation. On (b)(6), the patient went to take a nap. Her husband went to check on her and the patient was found to be deceased. Attempts to gather additional information have been unsuccessful. If additional information is received, a supplemental report will be submitted.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 1222780-2020-00053 |
MDR Report Key | 9809115 |
Report Source | COMPANY REPRESENTATIVE,HEALTH |
Date Received | 2020-03-09 |
Date of Report | 2020-02-18 |
Date of Event | 2020-02-14 |
Date Mfgr Received | 2020-02-18 |
Device Manufacturer Date | 2019-10-22 |
Date Added to Maude | 2020-03-09 |
Event Key | 0 |
Report Source Code | Manufacturer report |
Manufacturer Link | Y |
Number of Patients in Event | 0 |
Adverse Event Flag | 3 |
Product Problem Flag | 0 |
Reprocessed and Reused Flag | 3 |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 3 |
Event Location | 3 |
Manufacturer Contact | KELSEA LYVER |
Manufacturer Street | 250 CAMPUS DRIVE |
Manufacturer City | MARLBOROUGH, MA |
Manufacturer Country | US |
Manufacturer Phone | 2636130 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | NOVASURE IMPEDANCE CONTROLLED EA SYSTEM |
Generic Name | UTERINE ABLATION DEVICE |
Product Code | MNB |
Date Received | 2020-03-09 |
Model Number | NS2007 |
Catalog Number | NS2007 |
Lot Number | 19K22RD |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | HOLOGIC, INC |
Manufacturer Address | 250 CAMPUS DRIVE MARLBOROUGH, MA US |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Death | 2020-03-09 |