FDA Adverse Event Injury Summary report: N

MEDTRONIC PAIN PUMP

MDR report key: 112464 · Received July 18, 1997

Report

Report Number
112464
Event Type
Injury
Date Received
July 18, 1997
Date of Event
June 12, 1997
Report Date
July 14, 1997
Manufacturer
*
Product Code
LKK
Adverse Event
Yes
Report Source
User Facility report
Reporter Location
GA, US
Reporter Occupation
RISK MANAGER

Narratives

Description of Event or Problem · 1

BLOOD PRESSURE DROPPED FROM 220/103 TO NON-DETECTABLE. QUICKLY RECOVERED TO 86/24 (A-LINE 37/32).

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 MEDTRONIC PAIN PUMP Implant DILAUDID TOXICITY LKK * * *

Patients

Seq Age Sex Outcome Treatment
1 69 YR Hospitalization