FDA Adverse Event Injury Summary report: N

CVS DISINFECTING LENS CARE SOLUTION

MDR report key: 2991753 · Received March 6, 2013

Report

Report Number
2026940-2013-00001
Event Type
Injury
Date Received
March 6, 2013
Date of Event
January 24, 2013
Report Date
March 6, 2013
Manufacturer
KC PHARMACEUTICALS, INC.
Product Code
LPN
PMA / PMN Number
K010559
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

COMPLAINT SAMPLE COULD NOT BE RETRIEVED.

Description of Event or Problem · 1

ONE (1) PATIENT (CR-13-021) STATES THAT SHE EXPERIENCED IRRITATION AS WELL AS A BURNING SENSATION IN HER EYES AFTER USING A MEDICAL DEVICE, CVS DISINFECTING LENS CARE SOLUTION. THE PATIENT MEDICAL RECORD IS NOT AVAILABLE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
95849 CVS DISINFECTING LENS CARE SOLUTION LENS CARE SOLUTION LPN KC PHARMACEUTICALS, INC.

Patients

Seq Age Sex Outcome Treatment
1 Other