FDA Adverse Event Malfunction Summary report: N

CONSEPT 1 STEP NEUTRALIZING TABLETS

MDR report key: 1675766 · Received May 4, 2010

Report

Report Number
2020664-2008-00079
Event Type
Malfunction
Date Received
May 4, 2010
Date of Event
April 16, 2008
Report Date
May 22, 2008
Manufacturer
ABBOTT MEDICAL OPTICS, INC.
Product Code
LPN
Product Problem
Yes
Report Source
Manufacturer report
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

CUSTOMER RETURNED HIS LENS CASE WITH SOLUTION IN IT. THE SOLUTION WAS 1% HYDROGEN PEROXIDE. THE CUSTOMER'S NEUTRALIZING TABLETS WERE FOUND TO MEET SPECIFICATIONS. THE ROOT CAUSE HAS NOT BEEN ESTABLISHED.

Description of Event or Problem · 1

OUR OFFICE IN (B) (4) REPORTED MALE PATIENT EXPERIENCED EYE PAIN AFTER WEARING LENSES THAT HAD BEEN DISINFECTED/NEUTRALIZED WITH CONSEPT 1STEP. WHEN HE TRIED THE PRODUCT AGAIN HE HAD NO FURTHER PROBLEMS

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 CONSEPT 1 STEP NEUTRALIZING TABLETS LPN ABBOTT MEDICAL OPTICS, INC. NA 16462

Patients

Seq Age Sex Outcome Treatment
1 VENTED CONTACT LENS CASE| CONSEPT 1 STEP DISINFACTING SOLUTION