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 company representative report with the FDA on 2017-07-21 for 11G IVAS ACCESS CANNULA 0306330000 manufactured by Stryker Instruments-kalamazoo.

Event Text Entries

[80622130] It was reported that during a procedure the doctor was removing the cannula from the patient when the handle separated from the shaft. The stylet was successfully removed from the patient without the need for an incision. There was no significant clinical delay and no adverse consequences to the patient were reported.
Patient Sequence No: 1, Text Type: D, B5


[115093212] Device evaluation: we have evaluated the device.
Patient Sequence No: 1, Text Type: N, H10


[115093213] It was reported that during a procedure the doctor was removing the cannula from the patient when the handle separated from the shaft. The stylet was successfully removed from the patient without the need for an incision. There was no significant clinical delay and no adverse consequences to the patient were reported.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number0001811755-2017-01392
MDR Report Key6731178
Report SourceCOMPANY REPRESENTATIVE
Date Received2017-07-21
Date of Report2018-01-11
Date of Event2017-06-22
Date Mfgr Received2017-12-21
Device Manufacturer Date2016-08-30
Date Added to Maude2017-07-21
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. ZACHARY 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 HIGHWAY #3, KM 130.2
Manufacturer CityKALAMAZOO MI 49001
Manufacturer CountryUS
Manufacturer Postal Code49001
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 Received2017-07-21
Returned To Mfg2017-07-10
Catalog Number0306330000
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 KALAMAZOO MI 49001 US 49001


Patients

Patient NumberTreatmentOutcomeDate
10 2017-07-21

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