DISP NITINOL NDL SINGLE PACK N/A 110010851

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 2015-04-15 for DISP NITINOL NDL SINGLE PACK N/A 110010851 manufactured by Biomet Orthopedics.

Event Text Entries

[5673055] It was reported patient underwent a right rotator cuff repair procedure on (b)(6) 2015. During the procedure, the needle tip fractured after twelve to fifteen passes. Another needle was used and the tip fractured after twenty passes. Free and fixed needles were utilized to complete the procedure. It is unknown if patient retained a foreign body.
Patient Sequence No: 1, Text Type: D, B5


[13203218] Current information is insufficient to permit a conclusion as to the cause of the event. Review of device history records show that lot released with no complaint related anomaly or deviation.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number0001825034-2015-01513
MDR Report Key4695577
Report Source07
Date Received2015-04-15
Date of Report2015-03-18
Date of Event2015-03-17
Date Mfgr Received2015-03-18
Device Manufacturer Date2015-01-15
Date Added to Maude2015-04-16
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 Location0
Manufacturer ContactMS. MEGAN HAAS
Manufacturer Street56 E. BELL DRIVE
Manufacturer CityWARSAW IN 46582
Manufacturer CountryUS
Manufacturer Postal46582
Manufacturer Phone5743726700
Manufacturer G1BIOMET ORTHOPEDICS
Manufacturer Street56 E. BELL DRIVE
Manufacturer CityWARSAW IN 46582
Manufacturer CountryUS
Manufacturer Postal Code46582
Single Use3
Previous Use Code3
Removal Correction NumberN/A
Event Type3
Type of Report3

Device Details

Brand NameDISP NITINOL NDL SINGLE PACK
Generic NameSPORTS MED INSTRUMENTATION
Product CodeHXO
Date Received2015-04-15
Model NumberN/A
Catalog Number110010851
Lot Number990730
ID NumberN/A
OperatorPHYSICIAN
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerBIOMET ORTHOPEDICS
Manufacturer Address56 E. BELL DRIVE WARSAW IN 46582 US 46582


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2015-04-15

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