FDA Adverse Event Injury Summary report: N

MP-28 SOFPORT PLACEMENT SYSTEM

MDR report key: 2923262 · Received October 11, 2006

Report

Report Number
1920664-2006-01440
Event Type
Injury
Date Received
October 11, 2006
Date of Event
September 1, 2006
Report Date
September 15, 2006
Manufacturer
BAUSCH & LOMB
Product Code
MSS
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
TN, US
Reporter Occupation
UNKNOWN

Narratives

Description of Event or Problem · 1

WHILE INSERTING THE LENS INTO THE PATIENT'S EYE, THE LENS DID NOT EXIT CORRECTLY IN THE DELIVERY DEVICE. THE LENS WAS REMOVED AND REPLACED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 MP-28 SOFPORT PLACEMENT SYSTEM INTRAOCULAR LENS MSS BAUSCH & LOMB H610801

Patients

Seq Age Sex Outcome Treatment
1 Required Intervention