MEDLINE
Received Apr 7, 2026 · Event occurred Mar 11, 2026
Report 1423395-2026-00080 · MDR key 24801583
Device
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.