FDA Adverse Event Injury Summary report: N

ACCUGLIDE MICROKERATOME DISPOSABLE BLADE

MDR report key: 2573200 · Received May 18, 2010

Report

Report Number
1920664-2010-00136
Event Type
Injury
Date Received
May 18, 2010
Date of Event
March 19, 2010
Report Date
April 21, 2010
Manufacturer
BAUSCH & LOMB, INC.
Product Code
HNO
PMA / PMN Number
K913697
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
MO, US
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL

Narratives

Description of Event or Problem · 1

(B)(6) 2010, 1 DAY P/O LASIK OU. PT STATES OD IS A BIT FUZZIER THAN OS. PT NOTICES EYES ACHE AT TIMES VSC 20/50, 20/40. (B)(6) 2010, 2 DAYS P/O LASIK OU VA A LITTLE HAZY AND BETTER YESTERDAY. VSC 20/40, 20/30. (B)(6) 2010, POSSIBLE DLK. CONSULT WITH DR INCREASE PF TO QHR OU WHILE AWAKE, SEE DR TOMORROW A.M. (B)(6) 2010 STAGE 2 DLK, DISCUSSED WASH OUT TODAY, FOLLOW UP WITH DR. (B)(6). (B)(6) 2010, OD NOTE FLAP LIFT IRRIGATE FOR DLK PREP AND DRAPE, PROCAINE AND TETRACAINE. OD FIRST LIFT FLAP WITH SINSKEY, IRRIGATE BED AND BACK OF FLAP, SPONGE DRY AND WET PF 1% PLACE ON BED. EPI PUSHED BACK WITH TOOKE FLAP REPLACED, IRRIGATE, BCL. SAME PROCEDURE FOR OS. SLIT LAMP EXAM GOOD OU. DISCHARGE TO HOME (B)(6) 2010. (B)(6) 2010, PER AFFILIATE, PT HAS RETURNED TO BCVA 20/20.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 ACCUGLIDE MICROKERATOME DISPOSABLE BLADE REFRACTIVE PRODUCTS HNO BAUSCH & LOMB, INC. NA 1142317

Patients

Seq Age Sex Outcome Treatment
1 UNK Other