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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: JOHNSON & JOHNSON VISION CARE, INC. CONTACT LENSES; LENSES, SOFT CONTACT, DAILY WEAR
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JOHNSON & JOHNSON VISION CARE, INC. CONTACT LENSES; LENSES, SOFT CONTACT, DAILY WEAR Back to Search Results
Device Problem Adverse Event Without Identified Device or Use Problem (2993)
Patient Problem Vitreous Hemorrhage (2143)
Event Date 05/28/2020
Event Type  Injury  
Event Description
After i corrected the insurance situation, a prescription for contact lenses and solution were filled.As of (b)(6) 2021 no one at (b)(6) hospital' s 3 optometry departments can find a prescription for me.I have been told that my calls have been logged and the "missing" rx noted.When i received the new batch of lenses they caused my cornea to bleed.Later, in (b)(6), when i ran out of contact lenses after failing to obtain the prescription that temple u somehow filled, i resorted to using a pair that temple u gave me.My eyes bled again.During my detainment, i managed to call the fda and issue an adverse reaction complaint to both bausch and lomb and acuvue (johnson and johnson).I have the remaining drops of the saline solution as well as the packaging and sent that into b&l for forensics in (b)(6).This photo is the packaging with the lot numbers for the contact lenses given to me under a fraudulent prescription by dr.(b)(6) and the dispensary staff.
 
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Brand Name
CONTACT LENSES
Type of Device
LENSES, SOFT CONTACT, DAILY WEAR
Manufacturer (Section D)
JOHNSON & JOHNSON VISION CARE, INC.
MDR Report Key11412803
MDR Text Key238335113
Report NumberMW5099784
Device Sequence Number2
Product Code LPL
Combination Product (y/n)Y
Number of Events Reported1
Summary Report (Y/N)N
Report Source Voluntary
Reporter Occupation Patient
Type of Report Initial
Report Date 02/22/2021
2 Devices were Involved in the Event: 1   2  
1 Patient was Involved in the Event
Date FDA Received03/03/2021
Is this an Adverse Event Report? Yes
Is this a Product Problem Report? Yes
Device Operator No Information
Was Device Evaluated by Manufacturer? No Information
Type of Device Usage N
Patient Sequence Number1
Patient Outcome(s) Other; Disability;
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