CLOSED KNOT PUSHER N/A 902813

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 07 report with the FDA on 2010-09-09 for CLOSED KNOT PUSHER N/A 902813 manufactured by Biomet Sports Medicine, Inc..

Event Text Entries

[1704506] It was reported that patient underwent a procedure utilizing a closed knot pusher on (b)(6) 2010. During the procedure, the knot pusher cut a suture. An additional suture was implanted, but the knot pusher cut that one as well. The procedure was completed using a competitor's knot pusher.
Patient Sequence No: 1, Text Type: D, B5


[8702698] Closed knot pusher part 902813 lot 864100 subject of recall. (b)(4).
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number1825034-2010-00364
MDR Report Key1829334
Report Source07
Date Received2010-09-09
Date of Report2010-08-13
Date of Event2010-08-11
Date Facility Aware2010-09-01
Date Mfgr Received2010-08-13
Device Manufacturer Date2010-03-29
Date Added to Maude2010-09-09
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 FDA0
Event Location3
Manufacturer ContactMR. JEREMY SCHROEDER
Manufacturer Street56 E. BELL DRIVE P.O. BOX 587
Manufacturer CityWARSAW IN 46581
Manufacturer CountryUS
Manufacturer Postal46581
Manufacturer Phone5743713755
Manufacturer G1BIOMET SPORTS MEDICINE, INC.
Manufacturer Street56 E. BELL DRIVE P.O. BOX 587
Manufacturer CityWARSAW IN 46581
Manufacturer CountryUS
Manufacturer Postal Code46581
Single Use3
Remedial ActionRC
Previous Use Code3
Removal Correction NumberRES # 56589
Event Type3
Type of Report3

Device Details

Brand NameCLOSED KNOT PUSHER
Generic NamePUSHER, SOCKET
Product CodeHXO
Date Received2010-09-09
Returned To Mfg2010-08-20
Model NumberN/A
Catalog Number902813
Lot Number864100
OperatorPHYSICIAN
Device AvailabilityR
Device Age4 MO
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerBIOMET SPORTS MEDICINE, INC.
Manufacturer Address56 E. BELL DRIVE P.O. BOX 587 WARSAW IN 46581 US 46581


Patients

Patient NumberTreatmentOutcomeDate
10 2010-09-09

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