ACETAB PRESSURISER 52MM(5PACK) 3206052

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-03-12 for ACETAB PRESSURISER 52MM(5PACK) 3206052 manufactured by Depuy Orthopaedics Inc Us.

Event Text Entries

[138915498] If information is obtained that was not available for the initial medwatch, a follow-up medwatch will be filed as appropriate. Device was used for treatment, not diagnosis.
Patient Sequence No: 1, Text Type: N, H10


[138915499] It was reported that the acetabular pressure riser (p/n: (b)(4) was broken when it was attached to t handle for cementing the acetabular side during tha surgery on (b)(6) 2019. The surgery was completed by using the spare and there was within a 30 minutes surgical delay. There were no broken parts in the patient? S body and there was no adverse consequence to the patient. No further information is available.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1818910-2019-87045
MDR Report Key8413179
Date Received2019-03-12
Date of Report2019-02-19
Date of Event2019-02-19
Date Mfgr Received2019-07-12
Device Manufacturer Date2014-04-30
Date Added to Maude2019-03-12
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. KARA DITTY-BOVARD
Manufacturer Street1210 WARD AVENUE
Manufacturer CityWEST CHESTER PA 193800988
Manufacturer CountryUS
Manufacturer Postal193800988
Manufacturer Phone6103142063
Manufacturer G1DEPUY ORTHOPAEDICS, INC. 1818910
Manufacturer Street700 ORTHOPAEDIC DRIVE
Manufacturer CityWARSAW IN 465820988
Manufacturer CountryUS
Manufacturer Postal Code465820988
Single Use3
Previous Use Code3
Event Type3
Type of Report0

Device Details

Brand NameACETAB PRESSURISER 52MM(5PACK)
Generic NameDEPUY CMW CEMENTING ACCESSORIES : CEMENT DELIVERY DEVICES
Product CodeJDZ
Date Received2019-03-12
Catalog Number3206052
Lot Number60520353
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerDEPUY ORTHOPAEDICS INC US
Manufacturer Address700 ORTHOPAEDIC DRIVE WARSAW IN 465810988 US 465810988


Patients

Patient NumberTreatmentOutcomeDate
10 2019-03-12

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