BIO-TRANSFIX, 5MM X 50MM AR-1400TB

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05,06,07 report with the FDA on 2006-12-01 for BIO-TRANSFIX, 5MM X 50MM AR-1400TB manufactured by Arthrex, Inc..

Event Text Entries

[16716252] Pt presented with pain and swelling at insertion site after anterior cruciate ligament repair. Culture showed staph epidermidis present. Pt was administered vancomycin to treat the infection. Pt is to follow up with his general doctor. This device is used for treatment.
Patient Sequence No: 1, Text Type: D, B5


[16906549] It is unk if the implant was removed from the pt, dhr review revealed no issues with the sterilization of this product. Staph epidermidis is a common inhabitant of the skin. Infections reported with this organism are typically acquired in the hosp mainly through skin wounds and/or indwelled catheters. There are no other complaints for this part / lot number combination. This event is not considered a product related issue.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number1220246-2006-00177
MDR Report Key789978
Report Source05,06,07
Date Received2006-12-01
Date of Report2006-11-29
Date of Event2006-11-14
Date Mfgr Received2006-11-14
Device Manufacturer Date2006-04-01
Date Added to Maude2006-12-06
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 Location0
Manufacturer ContactIVETTE GALMEZ, SR. ANALYST
Manufacturer Street1370 CREEKSIDE BLVD
Manufacturer CityNAPLES FL 341081945
Manufacturer CountryUS
Manufacturer Postal341081945
Manufacturer Phone8009337001
Manufacturer G1*
Manufacturer Street*
Manufacturer City*
Manufacturer Country*
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameBIO-TRANSFIX, 5MM X 50MM
Generic NameBIO-ABSORBABLE FIXATION DEVICE
Product CodeMNU
Date Received2006-12-01
Model NumberNA
Catalog NumberAR-1400TB
Lot Number77889
ID NumberNA
Device Expiration Date2008-04-01
Device AvailabilityN
Device Eval'ed by MfgrN
Implant FlagY
Date RemovedA
Device Sequence No1
Device Event Key777656
ManufacturerARTHREX, INC.
Manufacturer Address* NAPLES FL * US
Baseline Brand NameSCREW, BIO-INTERFERENCE, 10X 28MM(FULL THREAD)
Baseline Generic NameBIO-ABSORBABLE FIXATION DEVICE
Baseline Model NoAR-1400TB
Baseline Catalog NoAR-1400TB
Baseline IDNA


Patients

Patient NumberTreatmentOutcomeDate
10 2006-12-01

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