FDA Adverse Event Injury Summary report: N

MEDICHOICE

MDR report key: 4253561 · Received November 7, 2014

Report

Report Number
MW5039073
Event Type
Injury
Date Received
November 7, 2014
Date of Event
October 13, 2014
Report Date
November 7, 2014
Manufacturer
PHILIPS BURTON
Product Code
KZF
Adverse Event
Yes
Report Source
Voluntary report
Reporter Location
IA, US
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL

Narratives

Description of Event or Problem · 1

PATIENT HAS BEEN SEEN IN CONVENIENT CARE FOR STITCHES. PATIENT WAS LYING ON EXAM TABLE AND PHYSICIAN MOVED THE PORTABLE (ON WHEELS) EXAM LIGHT CLOSER TO COMPLETE TREATMENT. EXAM LIGHT EASILY BECAME UNBALANCED AND FELL OVER ON PATIENT, STRIKING THEM IN THE MOUTH AND INJURING THE MOUTH (UPPER LIP) AND TEETH. PATIENT HAD LACERATION AND REFUSED STITCHES. PATIENT SUBSEQUENTLY WENT TO DENTIST AND MAY LOSE FRONT TEETH.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
719286 MEDICHOICE MOBILE EXAM LIGHT KZF PHILIPS BURTON LGHT7400A/LED
719287 MEDICHOICE MOBILE EXAM LIGHT KZF PHILIPS BURTON LGHT7400/LED

Patients

Seq Age Sex Outcome Treatment
1 54 YR Other