FDA Adverse Event Other Summary report: N

UNKNOWN

MDR report key: 2040194 · Received March 24, 2011

Report

Report Number
2028253-2011-00011
Event Type
Other
Date Received
March 24, 2011
Date of Event
June 5, 2009
Report Date
March 14, 2011
Manufacturer
BREG, INC
Product Code
ILO
PMA / PMN Number
UNKNOWN
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
TX, US
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 1

BREG RECEIVED LEGAL NOTICE OF LAWSUITS FOR 'UNK COLD THERAPY UNIT' ALLEGING "PERSONAL INJURY" AFTER USE OF COLD THERAPY. THE EXTENT OF THE "PERSONAL INJURY" IS UNK AND REPORTER HAS NO KNOWLEDGE IF THIS TERM MEETS THE REQUIREMENTS OF SERIOUS INJURY AS DEFINED BY CURRENT FDA GUIDELINES. BREG HAS REVIEWED INTERNAL COMPLAINT FILES AND MAUDE DATABASE AND FINDS NO RECORD OF PREVIOUS NOTICE OF THESE "PERSONAL INJURY" CLAIMS. FIRST NOTIFICATION WAS SERVICE OF LAWSUIT ON (B)(6) 2011.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 UNKNOWN 89ILO ILO BREG, INC UNKNOWN UNKNOWN

Patients

Seq Age Sex Outcome Treatment
1 Other