CURETTE * NL-6760-009

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2011-11-14 for CURETTE * NL-6760-009 manufactured by Cardinal V-mueller.

Event Text Entries

[19364119] Curette tip broke off during total right knee arthroplasty. Tip of curette sucked into suction container. There was no harm to the patient.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2350770
MDR Report Key2350770
Date Received2011-11-14
Date of Report2011-11-14
Date of Event2011-11-11
Report Date2011-11-14
Date Reported to FDA2011-11-14
Date Added to Maude2011-11-29
Event Key0
Report Source CodeUser Facility report
Manufacturer LinkN
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag0
Reprocessed and Reused Flag0
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Single Use0
Previous Use Code0
Event Type3
Type of Report3

Device Details

Brand NameCURETTE
Generic NameCURETTE, SURGICAL
Product CodeFZS
Date Received2011-11-14
Model Number*
Catalog NumberNL-6760-009
Lot Number*
ID Number*
OperatorPHYSICIAN
Device AvailabilityY
Device Sequence No1
Device Event Key0
ManufacturerCARDINAL V-MUELLER
Manufacturer Address1430 WAUKEGAN RD. MCGAW PARK IL 60085 US 60085


Patients

Patient NumberTreatmentOutcomeDate
10 2011-11-14

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