inforMED
InjuryEGJ

TRANSQ SM

Received Jul 2, 2009 · Event occurred Apr 21, 2009

Report 1721293-2009-00005 · MDR key 1410618

Device

Manufacturer

Empi

Model number

5000009

Catalog number

5000009

Product problems

  • Insufficient Device Problem Information

Patient

58 YR

  • Superficial (First Degree) Burn

Narrative

Additional Manufacturer Narrative

DEVICE NOT YET RECEIVED BY MANUFACTURER FOR INSPECTION AND EVALUATION. ANY ADDITIONAL INFORMATION THAT MAY BE OBTAINED WILL BE SENT IN A FOLLOW-UP WHEN AVAILABLE.

Description of Event or Problem

PATIENT RECEIVED BURNS DURING IONTOPHORESIS. BURNS CLASSIFIED AS 1ST DEGREE. MEDICATION DELIVERED THROUGH TREATMENT WAS KETOPROFEN, DOSAGE 2.0CC. PATIENT IS REPORTED AS HAVING NO PREEXISTING CONDITIONS. WAVE FORM USED FOR TREATMENT WAS CONSTANT CURRENT. INTENSITY WAS NOT DISCLOSED. TREATMENT WAS INTERRUPTED BUT PROGRESS TOWARD RECOVERY WAS NOT IMPEDED. PATIENT RECEIVED "LOCAL PHARMACOLOGIC TREATMENT" FOR BURN.