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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: BAUSCH & LOMB, INC. UP & UP MULTIPURPOSE SOLUTION ADVANCED FORMULA; ACCESSORIES, SOLUTION, ULTRASONIC CLEANERS FOR LENSES
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BAUSCH & LOMB, INC. UP & UP MULTIPURPOSE SOLUTION ADVANCED FORMULA; ACCESSORIES, SOLUTION, ULTRASONIC CLEANERS FOR LENSES Back to Search Results
Device Problem Patient-Device Incompatibility (2682)
Patient Problems Corneal Abrasion (1789); Corneal Clouding/Hazing (1878); Increased Sensitivity (2065); Burning Sensation (2146); Caustic/Chemical Burns (2549)
Event Date 02/25/2019
Event Type  No Answer Provided  
Event Description
I had switched contact solution and went to put my contacts in before work.My eyes starting burning to the point i was unable to open my eyes.When i finally was able to, i couldn¿t see ¿ my vision was hazy.I had chemical burns/corneal abrasions on both my eyes and both rather severe.I missed 2 days of work due to being unable to see to drive.It also caused light sensitivity.Chemical/corneal abrasions.Is the product compounded? yes.Is the product over-the-counter? yes.Did the problem stop after the person reduced the dose or stopped taking or using the product? yes.Frequency, as needed.How was it taken or used.Contact set in solution then put in eye.Date the person stopped taking or using the product, (b)(6) 2019.
 
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Brand Name
UP & UP MULTIPURPOSE SOLUTION ADVANCED FORMULA
Type of Device
ACCESSORIES, SOLUTION, ULTRASONIC CLEANERS FOR LENSES
Manufacturer (Section D)
BAUSCH & LOMB, INC.
MDR Report Key8394180
MDR Text Key138087843
Report NumberMW5084673
Device Sequence Number0
Product Code LPN
Combination Product (y/n)N
Reporter Country CodeUS
Number of Events Reported1
Summary Report (Y/N)N
Report Source Voluntary
Reporter Occupation Patient
Type of Report Initial
Report Date 03/04/2019
1 Device was Involved in the Event
1 Patient was Involved in the Event
Date FDA Received03/05/2019
Device Operator No Information
Was Device Available for Evaluation? No
Was Device Evaluated by Manufacturer? No Information
Type of Device Usage N
Patient Sequence Number1
Patient Outcome(s) Other;
Patient Age26 YR
Patient Weight104
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