FDA Adverse Event Injury Summary report: N

SOLETRA

MDR report key: 3240217 · Received July 22, 2013

Report

Report Number
3004209178-2013-12074
Event Type
Injury
Date Received
July 22, 2013
Report Date
June 25, 2013
Manufacturer
MEDTRONIC MED REL MEDTRONIC PUERTO RICO
Product Code
MHY
PMA / PMN Number
H020007
Adverse Event
Yes
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
AR, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

CONCOMITANT MEDICAL PRODUCTS: PRODUCT ID 7426, SERIAL# (B)(4), IMPLANTED: (B)(6) 2006. PRODUCT TYPE: IMPLANTABLE NEUROSTIMULATOR: PRODUCT ID 7482, SERIAL# (B)(4), IMPLANTED: (B)(6) 2006. PRODUCT TYPE: EXTENSION: PRODUCT ID 3387, LOT# V005849, IMPLANTED: (B)(6) 2006. PRODUCT TYPE: LEAD: PRODUCT ID 3387, LOT# V005849, IMPLANTED: (B)(6) 2006. PRODUCT TYPE: LEAD: PRODUCT ID 7482, SERIAL# (B)(4), IMPLANTED: (B)(6) 2006. PRODUCT TYPE: EXTENSION: PRODUCT ID 7438, SERIAL# (B)(4), IMPLANTED: (B)(6) 2006. PRODUCT TYPE: PROGRAMMER, PATIENT. (B)(4).

Additional Manufacturer Narrative · 1

(B)(4).

Description of Event or Problem · 1

ADDITIONAL INFORMATION RECEIVED REPORTED ALL HER COMPONENTS WERE TAKEN OUT BUT ONE WAS LEFT IN. THE PATIENT WAS TOLD IT WAS TOO DANGEROUS TO REMOVE THE COMPONENT BUT SHE DID NOT KNOW WHICH ONE. PER THE MANUFACTURER¿S DEVICE REGISTRY THE PATIENT¿S LEADS WERE NOT REMOVED.

Description of Event or Problem · 1

IT WAS REPORTED THE PATIENT¿S DEVICE SYSTEM WAS REMOVED SOMETIME IN 2006 OR EARLY 2007 BECAUSE IT WAS NOT WORKING SO HER PHYSICIAN DECIDED ON REMOVAL. IT WAS NOTED THE PATIENT CURRENTLY STILL HAD A LOT OF SHAKING AND TREMORS.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
339642 SOLETRA STIMULATOR, ELECTRICAL, IMPLANTED, FOR PARKINSONIAN TREMOR MHY MEDTRONIC MED REL MEDTRONIC PUERTO RICO 7426

Patients

Seq Age Sex Outcome Treatment
1 00052 YR Required Intervention