KERRISON BLK COATED 130 UP 230X3MM THIN FK926B

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 01,07 report with the FDA on 2014-09-04 for KERRISON BLK COATED 130 UP 230X3MM THIN FK926B manufactured by Aesculap Ag And Co. Kg.

Event Text Entries

[4857433] Country of complaint: united states; complaint states: 3mm kerrison jammed into a patient during surgery and broke.
Patient Sequence No: 1, Text Type: D, B5


[12310164] Us reporting agent notified on (b)(4) 2014; evaluation is ongoing.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number2916714-2014-00702
MDR Report Key4084980
Report Source01,07
Date Received2014-09-04
Date of Report2014-09-04
Date of Event2014-08-05
Date Mfgr Received2014-08-05
Date Added to Maude2014-09-18
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional0
Initial Report to FDA3
Report to FDA0
Event Location0
Manufacturer ContactMICHELLE LINK
Manufacturer Street615 LAMBERT POINTE DRIVE
Manufacturer CityHAZELWOOD MO 63042
Manufacturer CountryUS
Manufacturer Postal63042
Manufacturer Phone3145515938
Manufacturer G1AESCULAP AGANDCO KG
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 NameKERRISON BLK COATED 130 UP 230X3MM THIN
Generic NameBONE PUNCH
Product CodeGXJ
Date Received2014-09-04
Model NumberFK926B
Catalog NumberFK926B
Lot Number2692
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device AgeDA
Device Eval'ed by Mfgr*
Device Sequence No1
Device Event Key0
ManufacturerAESCULAP AG AND CO. KG
Manufacturer AddressTUTTLINGEN 78532 DA 78532


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2014-09-04

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