FDA Adverse Event Injury Summary report: N

*

MDR report key: 3795406 · Received April 21, 2014

Report

Report Number
3795406
Event Type
Injury
Date Received
April 21, 2014
Date of Event
April 1, 2014
Report Date
April 21, 2014
Manufacturer
GAYMAR INDUSTRIES, INC.
Product Code
ILO
Adverse Event
Yes
Product Problem
Yes
Report Source
User Facility report
Reporter Location
OK, US
Reporter Occupation
INVALID DATA

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
239561 * PACK, HOT OR COLD, WATER CIRCULATING ILO GAYMAR INDUSTRIES, INC. * *

Patients

Seq Age Sex Outcome Treatment
1 61 YR Other| R
2 *