MAUDE Adverse Event Report: JOHNSON & JOHNSON SURGICAL VISION, INC SOVEREIGN COMPACT CONSOLE; PHACOFRAGMENTATION UNIT

Model Number	CMP680300
Medical Device Problem Code	Adverse Event Without Identified Device or Use Problem (2993)
Health Effect - Clinical Codes	Corneal Edema (1791); No Code Available (3191)
Type of Reportable Event	Serious Injury
Additional Manufacturer Narrative
Date of event is unknown as it was not provided, best estimate date is (b)(6) 2015 to (b)(6) 2017.Initial reporter's telephone: (b)(6).(b)(4).The system was evaluated by a field service engineer.All modes of operation and calibrations were verified and no failures were detected.In addition, the field service engineer has followed 15 surgeries and during all the procedures the physician did not complain about the equipment performance.The unit complied with all factory settings.On (b)(6) the field service engineer has followed 15 surgeries and during all the procedures the physician did not complain about the equipment performance.A review of records related to the device including complaint trending, and risk documentation will be performed.Upon completion of this review, if there is any further relevant information obtained, a supplemental medwatch will be filed.All pertinent information available to johnson & johnson surgical vision, inc has been submitted.
Event or Problem Description
The surgery center reported corneal edema after cataract procedure using a phacoemulsification unit.The surgeon indicated a corneal transplant was required.The surgeon does not have further information about the patient or date of incident.

• Brand Name: SOVEREIGN COMPACT CONSOLE
• Common Device Name: PHACOFRAGMENTATION UNIT
• Manufacturer (Section D): JOHNSON & JOHNSON SURGICAL VISION, INC; santa ana CA
• MDR Report Key: 7448796
• Report Number: 3006695864-2018-00849
• Device Sequence Number: 19327084
• Product Code: HQC
• UDI-Device Identifier: 05050474514706
• UDI-Public: (01)05050474514706
• Combination Product (Y/N): N
• Initial Reporter Country: BR
• PMA/510(K) Number: K060366
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: foreign,health professional,u
• Initial Reporter Occupation: Physician
• Type of Report: Initial
• Report Date (Section B): 04/20/2018

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: No
• Operator of Device: Physician
• Device Model Number: CMP680300
• Was Device Available for Evaluation?: Yes
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 03/21/2018
• Initial Report FDA Received Date: 04/20/2018
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1
• Outcome Attributed to Adverse Event: Required Intervention