CUTTING PLIER F/WIRE 470MM LX164R

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-04-23 for CUTTING PLIER F/WIRE 470MM LX164R manufactured by Aesculap Ag.

Event Text Entries

[144971091] (b)(4). Manufacturing site evaluation: investigation on-going. Additional information / investigation results will be provided in a supplemental report.
Patient Sequence No: 1, Text Type: N, H10


[144971092] It was reported that there was an issue with the cutting plier. During an unspecified procedure, a portion of the cutting edge was broken off. It occurred when the instrument was being used to cut metal (bolt/rod). A surgical delay of 8 minutes was noted. An x-ray was taken to confirm that all pieces had been retrieved and none remained in the surgical field. Additional information was not provided.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number9610612-2019-00282
MDR Report Key8541703
Date Received2019-04-23
Date of Report2019-04-23
Date Facility Aware2019-04-17
Date Mfgr Received2019-04-05
Device Manufacturer Date2018-12-10
Date Added to Maude2019-04-23
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 ContactMS. NICOLE BROYLES
Manufacturer Street615 LAMBERT POINTE DRIVE
Manufacturer CityHAZELWOOD MO 63042
Manufacturer CountryUS
Manufacturer Postal63042
Manufacturer Phone3145515988
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 NameCUTTING PLIER F/WIRE 470MM
Generic NameGENERAL SURGICAL INSTRUMENTS
Product CodeHXZ
Date Received2019-04-23
Returned To Mfg2019-04-15
Model NumberLX164R
Catalog NumberLX164R
Lot Number4510196471
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerAESCULAP AG
Manufacturer AddressPO BOX 40 TUTTLINGEN, 78501 GM 78501


Patients

Patient NumberTreatmentOutcomeDate
10 2019-04-23

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