FDA Adverse Event Other Summary report: N

RSP SHOULDER

MDR report key: 2093732 · Received April 21, 2011

Report

Report Number
1644408-2011-00217
Event Type
Other
Date Received
April 21, 2011
Date of Event
April 11, 2011
Report Date
April 11, 2011
Manufacturer
ENCORE MEDICAL, L.P.
Product Code
KWS
PMA / PMN Number
K051075
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
MO, US
Reporter Occupation
NOT APPLICABLE

Narratives

Description of Event or Problem · 1

REVISION SURGERY - THE PT DISLOCATED, THE SURGEON EXCHANGED THE HUMERAL SHELLS.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 RSP SHOULDER HUMERAL SOCKET SHELL KWS ENCORE MEDICAL, L.P. 848C1072

Patients

Seq Age Sex Outcome Treatment
1 52 YR Required Intervention