LEEP PRIMA SPECULUM MED PSV-1L

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-03-05 for LEEP PRIMA SPECULUM MED PSV-1L manufactured by Coopersurgical, Inc..

Event Text Entries

[138119824] Coopersurgical, inc. Is currently investigating the reported condition. Once the investigation is complete, a follow up report will be filed. (b)(4).
Patient Sequence No: 1, Text Type: N, H10


[138119825] Issues with electricity which resulted in patient's vaginal wall burn.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1216677-2019-00115
MDR Report Key8392501
Date Received2019-03-05
Date of Report2019-02-21
Date of Event2019-02-14
Date Mfgr Received2019-02-21
Date Added to Maude2019-03-05
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 ContactMR. PETER NIZIOLEK
Manufacturer Street75 CORPORATE DRIVE
Manufacturer CityTRUMBULL CT 06611
Manufacturer CountryUS
Manufacturer Postal06611
Manufacturer G1COOPERSURGICAL, INC.
Manufacturer Street75 CORPORATE DRIVE
Manufacturer CityTRUMBULL CT 06611
Manufacturer CountryUS
Manufacturer Postal Code06611
Single Use3
Previous Use Code3
Event Type3
Type of Report0

Device Details

Brand NameLEEP PRIMA SPECULUM MED
Generic NameLEEP PRIMA SPECULUM MED
Product CodeHIB
Date Received2019-03-05
Returned To Mfg2019-02-21
Model NumberPSV-1L
Catalog NumberPSV-1L
Device AvailabilityR
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerCOOPERSURGICAL, INC.
Manufacturer Address75 CORPORATE DRIVE TRUMBULL CT 06611 US 06611


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2019-03-05

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