UNKNOWN CERCLAGE WIRE UNK_JR

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2018-06-11 for UNKNOWN CERCLAGE WIRE UNK_JR manufactured by Stryker Orthopaedics-mahwah.

Event Text Entries

[110705315] Additional information has been requested and if received will be provided in a supplemental report. Not returned.
Patient Sequence No: 1, Text Type: N, H10


[110705316] At the beginning of (b)(6) 2012 he was subjected to the removal of the metallic cerclage mobilized in the meantime.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number0002249697-2018-01772
MDR Report Key7588854
Date Received2018-06-11
Date of Report2018-06-11
Date of Event2012-05-01
Date Mfgr Received2018-05-16
Date Added to Maude2018-06-11
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. KEYLA COLON
Manufacturer Street325 CORPORATE DRIVE
Manufacturer CityMAHWAH NJ 07430
Manufacturer CountryUS
Manufacturer Postal07430
Manufacturer Phone2018315000
Manufacturer G1STRYKER ORTHOPAEDICS-MAHWAH
Manufacturer Street325 CORPORATE DRIVE
Manufacturer CityMAHWAH NJ 07430
Manufacturer CountryUS
Manufacturer Postal Code07430
Single Use3
Previous Use Code3
Event Type3
Type of Report0

Device Details

Brand NameUNKNOWN CERCLAGE WIRE
Generic NameUNKNOWN HIP IMPLANT
Product CodeHXN
Date Received2018-06-11
Catalog NumberUNK_JR
Lot NumberUNKNOWN
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerSTRYKER ORTHOPAEDICS-MAHWAH
Manufacturer Address325 CORPORATE DRIVE MAHWAH NJ 07430 US 07430


Patients

Patient NumberTreatmentOutcomeDate
101. Hospitalization; 2. Other; 3. Required No Informationntervention 2018-06-11

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