BERMANN MALLET 655GR.HEAD-D45MM 245MM FL060R

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2018-03-01 for BERMANN MALLET 655GR.HEAD-D45MM 245MM FL060R manufactured by Aesculap Ag.

Event Text Entries

[101481493] (b)(4). Manufacturing site evaluation: evaluation on-going.
Patient Sequence No: 1, Text Type: N, H10


[101481494] Country of complaint: usa. Mallet cracked while in use on patient. Use as intended in ortho case. No injury to patient. Delay in surgery reported.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number9610612-2018-00085
MDR Report Key7305777
Date Received2018-03-01
Date of Report2018-08-15
Date of Event2018-02-01
Date Facility Aware2018-02-16
Date Mfgr Received2018-02-02
Device Manufacturer Date2016-10-18
Date Added to Maude2018-03-01
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 NameBERMANN MALLET 655GR.HEAD-D45MM 245MM
Generic NameMALLETS
Product CodeHXL
Date Received2018-03-01
Returned To Mfg2018-02-21
Model NumberFL060R
Catalog NumberFL060R
Lot Number52278706
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device Age1 YR
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 2018-03-01

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