BIPASS DISPOSABLE NITINOL N/A 902092

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 2010-03-11 for BIPASS DISPOSABLE NITINOL N/A 902092 manufactured by Biomet Sports Medicine.

Event Text Entries

[1288701] It was reported that patient underwent a rotator cuff repair procedure utilizing a suture passer on (b)(6) 2010. During the procedure, the surgeon made unsuccessful attempts to pass the suture through the rotator cuff. The tip of the nitinol wire fractured but could not be located. Surgeon searched the joint space however, no radiographs were taken.
Patient Sequence No: 1, Text Type: D, B5


[8442496] Evaluation in process but not yet complete. Upon completion of evaluation, a follow up report will be sent to the fda. This report filed (b)(6) 2010.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number1825034-2010-00082
MDR Report Key1629070
Report Source07
Date Received2010-03-11
Date of Report2010-02-17
Date of Event2010-02-03
Date Facility Aware2010-03-11
Date Mfgr Received2010-02-17
Device Manufacturer Date2009-11-20
Date Added to Maude2010-11-17
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 ContactMRS. MIRANDA PARCELS
Manufacturer Street56 EAST BELL DRIVE P.O. BOX 587
Manufacturer CityWARSAW IN 465810587
Manufacturer CountryUS
Manufacturer Postal465810587
Manufacturer Phone5742676639
Manufacturer G1BIOMET SPORTS MEDICINE
Manufacturer Street56 EAST BELL DRIVE P.O. BOX 587
Manufacturer CityWARSAW IN 46581058
Manufacturer CountryUS
Manufacturer Postal Code46581 0587
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameBIPASS DISPOSABLE NITINOL
Generic NamePUSHER
Product CodeHXO
Date Received2010-03-11
Returned To Mfg2010-02-19
Model NumberN/A
Catalog Number902092
Lot Number592170
ID NumberN/A
Device Expiration Date2014-11-30
OperatorPHYSICIAN
Device AvailabilityR
Device Age2 MO
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerBIOMET SPORTS MEDICINE
Manufacturer Address56 EAST BELL DRIVE P.O. BOX 587 WARSAW IN 46581058 US 46581 0587


Patients

Patient NumberTreatmentOutcomeDate
10 2010-03-11

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