NOVASURE IMPEDANCE CONTROLLED EA SYSTEM NS2013

MAUDE Adverse Event Report

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 2020-01-16 for NOVASURE IMPEDANCE CONTROLLED EA SYSTEM NS2013 manufactured by Hologic, Inc.

Event Text Entries

[176866854] The device has not yet been returned therefore, a failure analysis of the complaint device cannot be completed. If the device is returned and 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


[176866855] Hologic received this complaint under medwatch reference # (b)(4) which was submitted by the user facility it was reported that "the device would not perform ablation" according to the physician. The physician obtained a second device and deployed the device without issue. Physician examined uterus and found a perforation at that time. No additional details available.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1222780-2020-00013
MDR Report Key9599374
Report SourceCOMPANY REPRESENTATIVE,HEALTH
Date Received2020-01-16
Date of Report2019-12-11
Date of Event2019-12-11
Date Mfgr Received2019-12-11
Device Manufacturer Date2019-10-10
Date Added to Maude2020-01-16
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactKELSEA LYVER
Manufacturer Street250 CAMPUS DRIVE
Manufacturer CityMARLBOROUGH MA 01752
Manufacturer CountryUS
Manufacturer Postal01752
Manufacturer Phone5082636130
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameNOVASURE IMPEDANCE CONTROLLED EA SYSTEM
Generic NameUTERINE ABLATION DEVICE
Product CodeMNB
Date Received2020-01-16
Model NumberNS2013
Catalog NumberNS2013
Lot Number19K10RD
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerHOLOGIC, INC
Manufacturer Address250 CAMPUS DRIVE MARLBOROUGH MA 01752 US 01752


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2020-01-16

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