BULLET NOSE GRASPER 5MM 310MM PO190R

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2017-10-25 for BULLET NOSE GRASPER 5MM 310MM PO190R manufactured by Aesculap Ag.

Event Text Entries

[90965325] (b)(4). Manufacturing site evaluation: evaluation on-going.
Patient Sequence No: 1, Text Type: N, H10


[90965326] Country of complaint: usa. It was reported that the handle broke during normal operation. Insulation shaft melted. No harm to the patient. There was a fifteen (15) minute delay in surgery.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number9610612-2017-00503
MDR Report Key6978206
Date Received2017-10-25
Date of Report2018-07-30
Date of Event2017-09-28
Date Facility Aware2017-10-05
Date Mfgr Received2017-09-29
Date Added to Maude2017-10-25
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 ContactMS. NICOLE BROYLES
Manufacturer Street615 LAMBERT POINTE DRIVE
Manufacturer CityHAZELWOOD MO 63042
Manufacturer CountryUS
Manufacturer Postal63042
Manufacturer G1AESCULAP AG
Manufacturer StreetPO BOX 40
Manufacturer CityTUTTLINGEN, 78501
Manufacturer CountryGM
Manufacturer Postal Code78501
Single Use3
Previous Use Code3
Event Type3
Type of Report0

Device Details

Brand NameBULLET NOSE GRASPER 5MM 310MM
Generic NameAE 02 504 19A
Product CodeKNF
Date Received2017-10-25
Returned To Mfg2017-10-23
Model NumberPO190R
Catalog NumberPO190R
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device AgeDA
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerAESCULAP AG
Manufacturer AddressPO BOX 40 TUTTLINGEN, 78501 GM 78501


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2017-10-25

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