MAUDE Adverse Event Report: JOHNSON & JOHNSON SURGICAL VISION, INC. UNKNOWN/NOT PROVIDED

Model Number UNKNOWN

Device Problem Crack (1135)

Patient Problem No Consequences Or Impact To Patient (2199)

Event Type  malfunction  

Manufacturer Narrative

Additional information: breakdown of the 2 events of is as follows: tip deformed 1, cartridge damaged, cosmetic, improperly loaded 1.Serial/lot numbers of suspect products: unknown 2.1 investigation was completed, and 1 investigation was pending from this period.1 cartridge damaged.In the investigations it was concluded that product met manufacturing release criteria and no product deficiency was identified.A review of records related to the device including labeling, 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.That was received during the time period that covers this voluntary malfunction summary report has been submitted.

Event Description

This report summarizes 2 malfunction events.The events were related to cartridge tip cracked or damaged.There were no patient injuries reported associated to the events.

Manufacturer Narrative

This correction mdr is being submitted to address inaccurate information in section f and g.4 date on the xml version of the previous submission caused by a software glitch in the transmission process.The internal non-conformance numbers for this software issue are nr-0148919 and capa-010215.

• Brand Name: UNKNOWN/NOT PROVIDED
• Type of Device: UNKNOWN/NOT PROVIDED
• Manufacturer (Section D): JOHNSON & JOHNSON SURGICAL VISION, INC.; 1700 e st andrew place; santa ana CA 92705
• MDR Report Key: 9650006
• MDR Text Key: 177131829
• Report Number: 2648035-2020-00099
• Device Sequence Number: 1
• Product Code: KYB
• UDI-Device Identifier: (01)UNKNOWN
• UDI-Public: (01)UNKNOWN
• Combination Product (y/n): Y
• PMA/PMN Number: K961242
• Number of Events Reported: 2
• Summary Report (Y/N): Y
• Report Source: Manufacturer
• Type of Report: Initial,Followup
• Report Date: 01/01/2005,10/28/2020

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: Yes
• Device Operator: No Information
• Device Model Number: UNKNOWN
• Was the Report Sent to FDA?: No
• Date Report Sent to FDA: 01/01/2005
• Date Report to Manufacturer: 01/10/2005
• Initial Date Manufacturer Received: 01/14/2005
• Initial Date FDA Received: 01/30/2020
• Supplement Dates Manufacturer Received: 10/25/2020
• Supplement Dates FDA Received: 10/28/2020
• Patient Sequence Number: 1