CARBON STEEL SCALPEL BLADES #15 BB515

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,foreig report with the FDA on 2019-04-12 for CARBON STEEL SCALPEL BLADES #15 BB515 manufactured by Aesculap Ag.

Event Text Entries

[141894821] (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


[141894822] It was reported that there was an issue with the scalpel blade. While attempting to insert a blade onto the handle, the assistant cut herself deeply in her thumb. The blade was noted to have "jumped" out of the packaging. It was reported that the assistant was doing well and in the healing process. Further information has been requested.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number9610612-2019-00269
MDR Report Key8511625
Report SourceCOMPANY REPRESENTATIVE,FOREIG
Date Received2019-04-12
Date of Report2019-04-12
Date of Event2019-03-26
Date Facility Aware2019-04-10
Date Mfgr Received2019-04-02
Device Manufacturer Date2018-01-04
Date Added to Maude2019-04-12
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 Report3

Device Details

Brand NameCARBON STEEL SCALPEL BLADES #15
Generic NameBASIC INSTRUMENTS
Product CodeGES
Date Received2019-04-12
Model NumberBB515
Catalog NumberBB515
Lot Number4509129959
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device Age14 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. Other 2019-04-12

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