FDA Adverse Event Injury Summary report: N

SWEET PICOTIP RX

MDR report key: 1041112 · Received May 8, 2008

Report

Report Number
2124215-2008-35008
Event Type
Injury
Date Received
May 8, 2008
Date of Event
April 7, 2005
Report Date
April 13, 2005
Manufacturer
CARDIAC PACEMAKERS, INC
Product Code
DTB
Removal / Correction Number
NA
Adverse Event
Yes
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
OK, US
Reporter Occupation
PHYSICIAN

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 SWEET PICOTIP RX IMPLANTABLE LEAD DTB CARDIAC PACEMAKERS, INC 4054 NA

Patients

Seq Age Sex Outcome Treatment
1 79 YR