OSTEO-FORCE VERTEBROPLASTY INJECTOR SET N/A HPIS-100

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2017-05-12 for OSTEO-FORCE VERTEBROPLASTY INJECTOR SET N/A HPIS-100 manufactured by Cook Inc.

Event Text Entries

[75310076] Product code: oar. (b)(4). The event is currently under investigation. A follow-up report will be sent upon conclusion.
Patient Sequence No: 1, Text Type: N, H10


[75310077] Customer reported that the osteo-force vertebroplasty injector set fractured during use. The medical team was able to disengage the plunger and manually expel the cement. There was no reported injury to the patient. No further information was provided relating to this report.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1820334-2017-01029
MDR Report Key6563414
Date Received2017-05-12
Date of Report2017-08-31
Date Mfgr Received2017-08-16
Date Added to Maude2017-05-12
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 ContactMR. LARRY POOL
Manufacturer Street750 DANIELS WAY
Manufacturer CityBLOOMINGTON IN 47404
Manufacturer CountryUS
Manufacturer Postal47404
Manufacturer Phone8123392235
Single Use3
Previous Use Code3
Event Type3
Type of Report0

Device Details

Brand NameOSTEO-FORCE VERTEBROPLASTY INJECTOR SET
Product CodeOAR
Date Received2017-05-12
Model NumberN/A
Catalog NumberHPIS-100
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device AgeDA
Device Eval'ed by Mfgr*
Device Sequence No1
Device Event Key0
ManufacturerCOOK INC
Manufacturer Address750 DANIELS WAY BLOOMINGTON IN 47404 US 47404


Patients

Patient NumberTreatmentOutcomeDate
10 2017-05-12

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