inforMED
InjuryOJK

MEDLINE

Received Apr 7, 2026 · Event occurred Mar 11, 2026

Report 1423395-2026-00080 · MDR key 24801583

Device

Generic name

Glaucoma Pack-lf

Catalog number

DYNJ0567839R

Product problems

  • Insufficient Device Problem Information

Patient

NA · Unknown

  • Corneal Abrasion

Narrative

Additional Manufacturer Narrative

ACCORDING TO THE CUSTOMER, "CORNEAL ABRASIONS" WERE REPORTED RELATED TO THE DRAPE IN THE PACK. NO ADDITIONAL DETAILS ARE AVAILABLE RELATED TO THE CUSTOMER REPORTED ISSUE. DESPITE MULTIPLE GOOD FAITH EFFORTS TO OBTAIN ADDITIONAL INFORMATION, THE CUSTOMER CONTACT WAS UNABLE OR UNWILLING TO PROVIDE FURTHER INCIDENT DETAILS TO THE MANUFACTURER. NO ADDITIONAL INFORMATION IS AVAILABLE. IT HAS BEEN DETERMINED THAT THE REPORTED EVENT CAUSED OR CONTRIBUTED TO SERIOUS INJURY, THEREFORE, THIS MEDWATCH IS BEING FILED. IF ANY FURTHER RELEVANT INFORMATION IS IDENTIFIED OR OBTAINED, A SUPPLEMENTAL MEDWATCH WILL BE SUBMITTED.

Description of Event or Problem

CORNEAL ABRASIONS.