ORTHOSORB 1 PIN 50X1.3MM KIT N/A 841070

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 2014-04-29 for ORTHOSORB 1 PIN 50X1.3MM KIT N/A 841070 manufactured by Biomet Orthopedics.

Event Text Entries

[4433255] It was reported patient underwent a bunion procedure on an unknown date. During the procedure the orthosorb pin broke. A piece of the pin fell into the patient's wound and was retrieved. Another orthosorb pin was used to complete the procedure.
Patient Sequence No: 1, Text Type: D, B5


[11827592] 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 recorded anomaly or deviation.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number0001825034-2014-03339
MDR Report Key3778162
Report Source07
Date Received2014-04-29
Date of Report2014-04-02
Date Mfgr Received2014-04-02
Device Manufacturer Date2013-01-31
Date Added to Maude2014-04-29
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 FDA0
Event Location0
Manufacturer ContactMS. AMANDA ZAJICEK
Manufacturer Street56 E. BELL DRIVE
Manufacturer CityWARSAW IN 46582
Manufacturer CountryUS
Manufacturer Postal46582
Manufacturer Phone5743726782
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 NameORTHOSORB 1 PIN 50X1.3MM KIT
Generic NamePIN, FIXATION, RESORBALE, HARD TISSUE
Product CodeOVZ
Date Received2014-04-29
Model NumberN/A
Catalog Number841070
Lot Number453618
ID NumberN/A
Device Expiration Date2018-01-31
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. Hospitalization; 2. Required No Informationntervention 2014-04-29

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