TC HEGAR NEEDLE HOLDER HVY- SERR240MM BM078R

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a foreign,health professional report with the FDA on 2019-01-22 for TC HEGAR NEEDLE HOLDER HVY- SERR240MM BM078R manufactured by Aesculap Ag.

Event Text Entries

[133750075] (b)(4). When additional information is received a follow up report will be submitted.
Patient Sequence No: 1, Text Type: N, H10


[133750076] It was reported by the healthcare professional "the carbide insert cracked during use. The failure occurred during a gynecology procedure. Post-operative x-ray examination showed no sign of foreign object in the patient's body. " it was noted as the first use of the device. Additional patient information has been requested. When additional information is received a follow up report will be submitted.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number9610612-2019-00037
MDR Report Key8267641
Report SourceFOREIGN,HEALTH PROFESSIONAL
Date Received2019-01-22
Date of Report2019-01-22
Date of Event2018-12-25
Date Facility Aware2019-01-16
Date Mfgr Received2018-12-26
Device Manufacturer Date2018-06-05
Date Added to Maude2019-01-22
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationOTHER HEALTH CARE PROFESSIONAL
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactMRS. 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 Report3

Device Details

Brand NameTC HEGAR NEEDLE HOLDER HVY- SERR240MM
Generic NameNEEDLE HOLDER, REUSABLE
Product CodeHXK
Date Received2019-01-22
Returned To Mfg2019-01-16
Model NumberBM078R
Catalog NumberBM078R
Lot Number4509599999
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device Age6 MO
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerAESCULAP AG
Manufacturer AddressPO BOX 40 TUTTLINGEN, 78501 GM 78501


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2019-01-22

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