KINSA UNK 72200239

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 01,07 report with the FDA on 2007-11-29 for KINSA UNK 72200239 manufactured by Smith & Nephew Inc., Endoscopy Div..

Event Text Entries

[19961404] The surgeon retracted insertion sleeve all the way back before hammering in the anchor. The anchor was fractured from hammering.
Patient Sequence No: 1, Text Type: D, B5


[20094651] .
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number1219602-2007-00300
MDR Report Key956947
Report Source01,07
Date Received2007-11-29
Date of Report2007-11-26
Date of Event2007-06-25
Date Facility Aware2007-06-25
Report Date2007-11-26
Date Mfgr Received2007-11-16
Date Added to Maude2008-02-29
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 ContactDONNA LANTEIGNE
Manufacturer Street150 MINUTEMAN RD
Manufacturer CityANDOVER MA 01810
Manufacturer CountryUS
Manufacturer Postal01810
Manufacturer Phone9787491576
Manufacturer G1SMITH & NEPHEW INC., ENDOSCOPY DIV.
Manufacturer Street130 FORBES BLVD.
Manufacturer CityMANSFIELD MA 02048
Manufacturer CountryUS
Manufacturer Postal Code02048
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameKINSA
Generic NameKINSA SUTURE ANCHOR
Product CodeKGS
Date Received2007-11-29
Model NumberUNK
Catalog Number72200239
Lot NumberUNK
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device AgeNA
Device Eval'ed by MfgrR
Implant FlagN
Date RemovedB
Device Sequence No1
Device Event Key953404
ManufacturerSMITH & NEPHEW INC., ENDOSCOPY DIV.
Manufacturer AddressMANSFIELD MA US


Patients

Patient NumberTreatmentOutcomeDate
10 2007-11-29

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