FDA Adverse Event Other Summary report: N

NOT REPORTED

MDR report key: 251852 · Received November 17, 1999

Report

Report Number
1928508-1999-00003
Event Type
Other
Date Received
November 17, 1999
Report Date
November 17, 1999
Manufacturer
M-PACT
Product Code
LGH
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
CA, US
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 1

BURN BLISTER 1 1/2 X 2 1/4 INCHES ON BACK OF KNEE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 NOT REPORTED PLASTER SPLINTING LGH M-PACT UNK UNK

Patients

Seq Age Sex Outcome Treatment
1 NO INFO Other NYLON HOSE.