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 2018-03-21 for 11G IVAS ACCESS CANNULA 0306330000 manufactured by Stryker Instruments-kalamazoo.

Event Text Entries

[103025377] Device discarded by customer.
Patient Sequence No: 1, Text Type: N, H10


[103025378] It was reported that during a procedure, the needle broke off in the patient. The physician initially used clamps to remove the device material from the patient without reinserting the stylet and bent the cannula. After an additional incision was made next to the placement of the cannula, the physician reinserted the stylet and successfully removed the device material from the patient. There was no clinically significant delay, no further adverse consequences to the patient, and the procedure was successfully completed.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number0001811755-2018-00528
MDR Report Key7357281
Report SourceCOMPANY REPRESENTATIVE
Date Received2018-03-21
Date of Report2018-03-21
Date of Event2018-02-22
Date Mfgr Received2018-02-22
Date Added to Maude2018-03-21
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
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 Received2018-03-21
Catalog Number0306330000
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerSTRYKER INSTRUMENTS-KALAMAZOO
Manufacturer Address4100 EAST MILHAM AVENUE KALAMAZOO MI 49001 US 49001


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2018-03-21

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