• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

MDR Database Search

  • Print
  • Share
  • E-mail
-
Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 

New SearchBack To Search Results
BRAND NAMEOCCASIONS MULTIFOCAL (POLYMACON) CONTACT LENS
BAUSCH & LOMB
1400 N. GOODMAN ST.
ROCHESTER NY
ACCESS NUMBERM571001
PRODUCT CODELPL
PANELOPHTHALMIC
REPORT TYPESERIOUS INJURY
DATE FDA RECEIVED10/15/1994
EVENT DESCRIPTION TYPEFINAL
EVENT DESCRIPTION
PATIENT IS AN EXPERIENCED CONTACT LENS WEARER. SHE WAS REFIT INTO THIS BIFOCALCONTACT LENS AND AFTER THREE DAYS OF USE, SHE NOTICED DIMINISHING ACUITY AND THAT HER RIGHT LENS WOULD BOTHER HER BY THE END OF THE DAY. SHE CONTINUED TO WEAR THE LENS FOR ANOTHER WEEK AND THEN WENT TO HER EYE CARE PRACTITIONER. SHE WAS REFERRED TO AN OPHTHALMOLOGIST WHO DIAGNOSED A CORNEAL ABRASION O.D. THE ABRASIONHEALED WITH TREATMENT AND THE PATIENT RESUMED LENS WEAR WITH A NEW LENS. THE DISPENSER LOOKED AT THE LENS IN QUESTION, SAW NOTHING VISIBLY WRONG AND THREW ITAWAY.
-
-