MAUDE Adverse Event Report: JOHNSON & JOHNSON SURGICAL VISION, INC. INTRAOCULAR LENS

Patient Problems Eye Infections (4466); Unspecified Eye / Vision Problem (4471)

Event Type  Other  

Event Description

To whom it may concern: i am sending you this letter to let you know i had cataract surgery in (b)(6) of this year which did not go so well.I have had an eye infection ever since then.My eye doctor put me on an antiobiotic and my pcp (primary care physician) put me on the same antibiotic in (b)(6) of this year.My eye doctor put me on a different antibiotic which worked to cure the infection.I believe the intraocular lens is the problem.The intraocular lens is from johnson & johnson vision care.I had the same surgery done in 2020 on the right, which is okay; it is just my left eye.I am going to try for a second opinion.I have sent a letter to johnson & johnson about this.Thank you for your cooperation in this matter.My left eye is getting in my way of driving.

• Brand Name: INTRAOCULAR LENS
• Type of Device: INTRAOCULAR LENS
• Manufacturer (Section D): JOHNSON & JOHNSON SURGICAL VISION, INC.
• MDR Report Key: 18319040
• MDR Text Key: 330477887
• Report Number: MW5149180
• Device Sequence Number: 1
• Product Code: HQL
• Combination Product (y/n): N
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Voluntary
• Reporter Occupation: Patient
• Type of Report: Initial
• Report Date: 11/28/2023

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Date FDA Received: 12/12/2023
• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: No
• Patient Sequence Number: 1
• Treatment: ¿ANTIBIOTIC¿