10G VERTEPORT CEMENT CANNULA (18/PKG) 0306410000

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative report with the FDA on 2018-11-21 for 10G VERTEPORT CEMENT CANNULA (18/PKG) 0306410000 manufactured by Stryker Instruments-kalamazoo.

Event Text Entries

[128098148] It was reported that the sterile packaging tore down sideways upon opening the device and contaminated the product. There was no associated procedure and therefore, no patient involvement.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number0001811755-2018-02539
MDR Report Key8096209
Report SourceCOMPANY REPRESENTATIVE
Date Received2018-11-21
Date of Report2018-11-21
Date of Event2018-10-29
Date Mfgr Received2018-10-29
Date Added to Maude2018-11-21
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. ZACH BAKER
Manufacturer Street4100 EAST MILHAM AVENUE
Manufacturer CityKALAMAZOO MI 49001
Manufacturer CountryUS
Manufacturer Postal49001
Manufacturer Phone2693237700
Manufacturer G1STRYKER INSTRUMENTS-KALAMAZOO
Manufacturer Street4100 EAST MILHAM AVENUE
Manufacturer CityKALAMAZOO MI 49001
Manufacturer CountryUS
Manufacturer Postal Code49001
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand Name10G VERTEPORT CEMENT CANNULA (18/PKG)
Generic NameINJECTOR, VERTEBROPLASTY
Product CodeOAR
Date Received2018-11-21
Catalog Number0306410000
Device AvailabilityY
Device AgeDA
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerSTRYKER INSTRUMENTS-KALAMAZOO
Manufacturer Address4100 EAST MILHAM AVENUE KALAMAZOO MI 49001 US 49001


Patients

Patient NumberTreatmentOutcomeDate
10 2018-11-21

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