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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: ALCON LABORATORIES, INC. CLEAR CARE
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ALCON LABORATORIES, INC. CLEAR CARE Back to Search Results
Device Problems Improper or Incorrect Procedure or Method (2017); Device Handling Problem (3265)
Patient Problems Irritation (1941); Pain (1994); Burning Sensation (2146)
Event Type  No Answer Provided  
Event Description
Hello, my name is (b)(6), i am a (b)(6) woman.This morning i was late for work and was rushing to get ready not only myself but my (b)(6) also.I just recently switched to daily contacts within the last 8 months or so, because my eyes were getting irritated with the monthly's.So i go to put my contacts in and one falls in the sink.I pick it up and go to quickly grab my contact solution to clean it off out of the drawer and accidently grabbed the cleaner (not thinking it was the same size and shape as my solution).I go to put my contact back in my eye and all hell broke loose.My eye was in excruciating pain (i've had 2 - (b)(6).Children with no drugs.) one of the worst pains i have experienced.Nothing like having a chemical burn in your eye to start your day.Mind you it was my error in not looking closely to the product before putting something in my eye, but as a suggestion and a plea to avoid this in the future, please change the shape of the bottle.The warnings on the bottle do not help if you have poor eyesight.Muscle memory is a big thing with humans.Unhappily, (b)(6).(b)(4).
 
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Brand Name
CLEAR CARE
Type of Device
CLEAR CARE
Manufacturer (Section D)
ALCON LABORATORIES, INC.
MDR Report Key6947529
MDR Text Key89461565
Report NumberMW5072741
Device Sequence Number1
Product Code LPN
Combination Product (y/n)N
Number of Events Reported1
Summary Report (Y/N)N
Report Source Voluntary
Reporter Occupation Patient
Type of Report Initial
1 Device was Involved in the Event
1 Patient was Involved in the Event
Date FDA Received10/13/2017
Is this an Adverse Event Report? No
Is this a Product Problem Report? No
Device Operator No Information
Was Device Evaluated by Manufacturer? No Information
Type of Device Usage N
Patient Sequence Number1
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