CHONDRAL PICK 40 DEG SMALL DIA 72201885

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,foreig report with the FDA on 2020-03-01 for CHONDRAL PICK 40 DEG SMALL DIA 72201885 manufactured by Smith & Nephew, Inc..

Event Text Entries

[181965174] It was reported that during surgery, when the 40 degree chondral pick was used, the device was brittle and the tip of it bent easily 90 degree. It is unknown whether there was a delay in the case. The procedure was completed with a competitor device. No patient injuries reported. All available information has been disclosed. If additional information should become available, a supplemental report will be submitted accordingly.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1219602-2020-00443
MDR Report Key9772665
Report SourceCOMPANY REPRESENTATIVE,FOREIG
Date Received2020-03-01
Date of Report2020-04-02
Date of Event2020-01-21
Date Mfgr Received2020-03-31
Device Manufacturer Date2017-10-26
Date Added to Maude2020-03-01
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 ContactHOLLY TOPPING
Manufacturer Street7000 WEST WILLIAM CANNON DRIVE
Manufacturer CityAUSTIN TX 78735
Manufacturer CountryUS
Manufacturer Postal78735
Manufacturer Phone5123913905
Manufacturer G1SMITH & NEPHEW, INC.
Manufacturer Street130 FORBES BOULEVARD
Manufacturer CityMANSFIELD MA 02048
Manufacturer CountryUS
Manufacturer Postal Code02048
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameCHONDRAL PICK 40 DEG SMALL DIA
Generic NameACCESSORIES,ARTHROSCOPIC
Product CodeNBH
Date Received2020-03-01
Returned To Mfg2020-02-19
Model Number72201885
Catalog Number72201885
Lot Number50693308
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device AgeDA
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerSMITH & NEPHEW, INC.
Manufacturer Address130 FORBES BOULEVARD MANSFIELD MA 02048 US 02048


Patients

Patient NumberTreatmentOutcomeDate
10 2020-03-01

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