FDA Adverse Event Malfunction Summary report: N

SYRINGE - 5CC LUER LOCK

MDR report key: 5986601 · Received September 27, 2016

Report

Report Number
MW5065083
Event Type
Malfunction
Date Received
September 27, 2016
Date of Event
June 23, 2016
Report Date
September 27, 2016
Manufacturer
INTERNATIONAL MEDISURG CONNECTION INC.
Product Code
FMF
Product Problem
Yes
Report Source
Voluntary report
Reporter Location
IL, US
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL

Narratives

Description of Event or Problem · 1

THE SYRINGE HAD A CRACK RESULTING IN THE PHYSICIAN GETTING SPRAYED IN THE EYE WITH A SALINE SOLUTION (WENT UNDER THE GOGGLES).

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
633263 SYRINGE - 5CC LUER LOCK SYRINGE - 5CC LUER LOCK FMF INTERNATIONAL MEDISURG CONNECTION INC. 13-7814-1

Patients

Seq Age Sex Outcome Treatment
1