FDA Adverse Event Injury Summary report: N

UNKNOWN LEFT ABGII HIP STEM

MDR report key: 2912807 · Received January 8, 2013

Report

Report Number
9616680-2013-90055
Event Type
Injury
Date Received
January 8, 2013
Date of Event
July 1, 2012
Report Date
December 13, 2012
Manufacturer
STRYKER ORTHOPAEDICS CORK
Product Code
KWY
PMA / PMN Number
UNK
Removal / Correction Number
NA
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
KY, US
Reporter Occupation
NOT APPLICABLE

Narratives

Additional Manufacturer Narrative · 1

ADDITIONAL INFO HAS BEEN REQUESTED AND IF RECEIVED, WILL BE PROVIDED IN A SUPPLEMENTAL REPORT.

Description of Event or Problem · 1

IT WAS REPORTED THAT THE PT IS EXPERIENCING SHARP PAIN IN HIS HIP JOINT. PT IS REPORTING NO SWELLING.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
10264 UNKNOWN LEFT ABGII HIP STEM IMPLANT KWY STRYKER ORTHOPAEDICS CORK NA UNK

Patients

Seq Age Sex Outcome Treatment
1 58 YR Other