WECK

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2013-03-12 for WECK manufactured by Pilling Weck.

Event Text Entries

[22046375] #2 weck curette introduced into uterus during d&c. Curette was retrieved and noted to be missing loop end. Xray performed and foreign body not seen. Tip found in plastic gyn bag by circulating nurse.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report NumberMW5029367
MDR Report Key3010675
Date Received2013-03-12
Date of Report2013-03-12
Date of Event2013-03-11
Date Added to Maude2013-03-20
Event Key0
Report Source CodeVoluntary report
Manufacturer LinkN
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationRISK MANAGER
Health Professional3
Initial Report to FDA3
Report to FDA0
Event Location0
Single Use0
Previous Use Code0
Event Type3
Type of Report3

Device Details

Brand NameWECK
Generic NameCURRETTE #2
Product CodeHHK
Date Received2013-03-12
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device Sequence No1
Device Event Key0
ManufacturerPILLING WECK
Manufacturer Address4024 STIRRUP CREEK RESEARCH TRIANGLE PARK NC 27703 US 27703


Patients

Patient NumberTreatmentOutcomeDate
101. Hospitalization 2013-03-12

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