MAGNUM CORE BIOPSY NEEDLES MN1410

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2020-01-15 for MAGNUM CORE BIOPSY NEEDLES MN1410 manufactured by Bard Peripheral Vascular, Inc..

Event Text Entries

[179310641] For the reported event, lot number was not provided. The sample was returned for evaluation. The company is still investigating the issue at this time. The device is labeled for single use.
Patient Sequence No: 1, Text Type: N, H10


[179310642] This report summarizes one malfunction. A review of the reported information indicated that model mn1410. Biopsy instrument allegedly experienced a break. This report was received from a single source. This event did involve patient with no reported patient injury. Age, weight, and gender were not provided for the patient.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2020394-2020-00272
MDR Report Key9591062
Date Received2020-01-15
Date of Report2020-03-31
Date Mfgr Received2020-03-26
Date Added to Maude2020-01-15
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 Location3
Manufacturer ContactJUDITH LUDWIG
Manufacturer Street1415 W. 3RD STREET
Manufacturer CityTEMPE AZ 85281
Manufacturer CountryUS
Manufacturer Postal85281
Manufacturer Phone4803032689
Manufacturer G1BARD REYNOSA S.A. DE C.V.
Manufacturer StreetBLVD MONTEBELLO #1 PARQUE INDUSTRIAL COLONIAL
Manufacturer CityREYNOSA TAMAULIPAS 88780
Manufacturer CountryMX
Manufacturer Postal Code88780
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameMAGNUM CORE BIOPSY NEEDLES
Generic NameBIOPSY INSTRUMENT
Product CodeFCG
Date Received2020-01-15
Model NumberMN1410
Catalog NumberMN1410
Lot NumberUNKNOWN
Device Availability*
Device AgeDA
Device Eval'ed by Mfgr*
Device Sequence No1
Device Event Key0
ManufacturerBARD PERIPHERAL VASCULAR, INC.
Manufacturer Address1625 W 3RD ST. TEMPE AZ 85281 US 85281


Patients

Patient NumberTreatmentOutcomeDate
10 2020-01-15

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