inforMED
MalfunctionMAL

HEMASHIELD PLATINUM WOVEN AORTIC ARCH 1B

Received Oct 7, 2022 · Event occurred Sep 14, 2022

Report 1640201-2022-00028 · MDR key 15560044

Device

Generic name

Graft, Vascular, Synthetic/biologic Composite

Manufacturer

Intervascular Sas

Model number

M00202175826P0

Catalog number

M00202175826P0

Lot number

21B17

Product problems

  • Product Quality Problem
  • Product Quality Problem

Patient

Prefer Not To Disclose

  • No Clinical Signs, Symptoms or Conditions
  • No Clinical Signs, Symptoms or Conditions

Narrative

Description of Event or Problem

COMPLAINT # (B)(4).

Additional Manufacturer Narrative

(10/213) THE INVOLVED DEVICE WAS RETURNED TO INTERVASCULAR ON 27-SEPT-2022 FOR EXAMINATION. A VISUAL INSPECTION BY A QUALIFIED QUALITY CONTROL TECHNICIAN WAS PERFORMED, THE CONCLUSION IS AS FOLLOW: "NO IDENTIFIED DEFAULT; NO LACK OF COLLAGEN IDENTIFICATION OF WHITE AND YELLOW STAINS IN RELATION WITH THE COLLAGEN.". (67) THE CONDUCTED INVESTIGATION CONCLUDES THAT THE PRODUCT WAS CONFORM TO THE SPECIFICATION.

Additional Manufacturer Narrative

(B)(4).

Description of Event or Problem

IT WAS REPORTING TO INTERVASCULAR THAT WHILE PREPARING FOR THE AORTIC DISSECTION SURGERY, A DISCOLORED AREA WAS DISCOVERED WITH MELTED COLLAGEN IN THE PRODUCT. THE OPERATION WAS COMPLETED WITH ANOTHER PRODUCT OF THE SAME MODEL STOCKED IN THE HOSPITAL. COMPLAINT (B)(4). PLEASE NOTE THAT THIS COMPLAINT IS ONE OF A SERIES OF TWO COMPLAINTS, THE SECOND COMPLAINT (B)(4) IS ALSO THE SUBJECT OF AN INITIAL EMDR REPORTING.