11G IVAS ACCESS CANNULA 0306330000

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a user facility report with the FDA on 2016-09-20 for 11G IVAS ACCESS CANNULA 0306330000 manufactured by Stryker Instruments-kalamazoo.

Event Text Entries

[55173927] It was reported that during a surgical procedure at the user facility that the handle of the access cannula separated while removing the cannula from the patient. The needle was successfully removed. No medical intervention, surgical delay, or adverse consequences were reported with this event.
Patient Sequence No: 1, Text Type: D, B5


[58389244]
Patient Sequence No: 1, Text Type: N, H10


[58389405] It was reported that during a surgical procedure at the user facility that the handle of the access cannula separated while removing the cannula from the patient. The needle was successfully removed. No medical intervention, surgical delay, or adverse consequences were reported with this event.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number0001811755-2016-02305
MDR Report Key5964056
Report SourceUSER FACILITY
Date Received2016-09-20
Date of Report2016-08-23
Date of Event2016-08-23
Date Mfgr Received2016-10-06
Date Added to Maude2016-09-20
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. CASEY METZGER
Manufacturer Street4100 EAST MILHAM AVENUE
Manufacturer CityKALAMAZOO MI 49001
Manufacturer CountryUS
Manufacturer Postal49001
Manufacturer Phone2693237700
Manufacturer G1STRYKER INSTRUMENTS-PUERTO RICO
Manufacturer StreetLAS PALMAS INDUSTRIAL PARK HIGHWAY #3, KM 130.2
Manufacturer CityARROYO 00615
Manufacturer Postal Code00615
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand Name11G IVAS ACCESS CANNULA
Generic NameINJECTOR, VERTEBROPLASTY (DOES NOT CONTAIN CEMENT)
Product CodeOAR
Date Received2016-09-20
Returned To Mfg2016-09-07
Catalog Number0306330000
Lot NumberUNKNOWN
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device AgeDA
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerSTRYKER INSTRUMENTS-KALAMAZOO
Manufacturer Address4100 EAST MILHAM AVENUE HIGHWAY #3, KM 130.2 KALAMAZOO MI 49001 US 49001


Patients

Patient NumberTreatmentOutcomeDate
10 2016-09-20

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