Hemashield M00202175828P0Recalls & reported problems
Intervascular Sas · Hemashield Platinum Woven 1 Branch Aortic Arch Double Velour Vascular Graft with Graft Sizer Accessory · Class 2 · Implant
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00384401018575), received between Sep 16, 2025 and Jan 9, 2026 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Improper or Incorrect Procedure or Method” (1 report).
20 other recalls cover devices cleared under the same FDA submission (K021213); they may or may not involve this specific model.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Improper or Incorrect Procedure or Method1
- Material Frayed1
- Product Quality Problem1
Patient problems
- No Clinical Signs, Symptoms or Conditions2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionJan 9, 2026Product Quality Problem
IT WAS REPORTED TO INTERVASCULAR THAT DURING AN ASCENDING AORTA REPLACEMENT PROCEDURE, CHANGES SUGGESTIVE OF COLLAGEN DISSOLUTION WERE NOTED ON THE GRAFT SURFACE DURING TRIMMING. THE GRAFT WAS THEREFORE REPLACED WITH A NEW ONE, AND THE PROCEDURE WAS COMPLETED WITHOUT FURTHER ISSUES. THE AFFECTED GRAFT IS AVAILABLE FOR RETURN UPON REQUEST.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24017667 ↗MalfunctionSep 16, 2025Material Frayed; Improper or Incorrect Procedure or Method; Material Frayed; Improper or Incorrect Procedure or Method
COMPLAINT # (B)(4).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23063288 ↗
Recalls under the same FDA submission
These recalls involve devices cleared under K021213. One submission often covers many models, so check the product and lot details in each record.
- Z-1874-2020 · Apr 7, 2020 · TerminatedHEMASHIELD PLATINUM Woven Double Velour Vascular Graft-1 Branch, Product Code: M00202175832P0 - Product Usage: for use in the replacement or repair of arteries affected with aneury
- Z-1876-2020 · Apr 7, 2020 · TerminatedHEMASHIELD PLATINUM Woven Double Velour Vascular Graft-3 Branch, Product Code: M00202175912P0 - Product Usage: for use in the replacement or repair of arteries affected with aneury
- Z-1881-2020 · Apr 7, 2020 · TerminatedHEMASHIELD PLATINUM Woven Double Velour Vascular Graft- 4 Branch, Product Code: M00202175928P0 - Product Usage: for use in the replacement or repair of arteries affected with aneur
- Z-1882-2020 · Apr 7, 2020 · TerminatedHEMASHIELD PLATINUM Woven Double Velour Vascular Graft-4 Branch, Product Code: M00202175930P0 - Product Usage: for use in the replacement or repair of arteries affected with aneury
- Z-1879-2020 · Apr 7, 2020 · TerminatedHEMASHIELD PLATINUM Woven Double Velour Vascular Graft-4 Branch, Product Code: M00202175924P0 - Product Usage: for use in the replacement or repair of arteries affected with aneury
- Z-1870-2020 · Apr 7, 2020 · TerminatedHEMASHIELD PLATINUM Woven Double Velour Vascular Graft- 1 Branch, Product Code: M00202175824P0 - Product Usage: for use in the replacement or repair of arteries affected with aneur
- Z-1877-2020 · Apr 7, 2020 · TerminatedHEMASHIELD PLATINUM Woven Double Velour Vascular Graft-3 Branch, Product Code: M00202175914P0 - Product Usage: for use in the replacement or repair of arteries affected with aneury
- Z-1878-2020 · Apr 7, 2020 · TerminatedHEMASHIELD PLATINUM Woven Double Velour Vascular Graft-4 Branch, Product Code: M00202175922P0 - Product Usage: for use in the replacement or repair of arteries affected with aneury
- Z-1864-2020 · Apr 7, 2020 · TerminatedHEMASHIELD PLATINUM Woven Double Velour Vascular Graft-Angled 4 Branch, Product Code: M00202175728AP0 - Product Usage: for use in the replacement or repair of arteries affected wit
- Z-1869-2020 · Apr 7, 2020 · TerminatedHEMASHIELD PLATINUM Woven Double Velour Vascular Graft- 1 Branch, Product Code: M00202175822P0 - Product Usage: for use in the replacement or repair of arteries affected with aneur
- Z-1880-2020 · Apr 7, 2020 · TerminatedHEMASHIELD PLATINUM Woven Double Velour Vascular Graft-4 Branch, Product Code: M00202175926P0 - Product Usage: for use in the replacement or repair of arteries affected with aneury
- Z-1867-2020 · Apr 7, 2020 · TerminatedHEMASHIELD PLATINUM Woven Double Velour Vascular Graft- 4 Branch, Product Code: M00202175734P0 - Product Usage: for use in the replacement or repair of arteries affected with aneur
- Z-1868-2020 · Apr 7, 2020 · TerminatedHEMASHIELD PLATINUM Woven Double Velour Vascular Graft- 1 Branch, Product Code: M00202175820P0 - Product Usage: for use in the replacement or repair of arteries affected with aneur
- Z-1875-2020 · Apr 7, 2020 · TerminatedHEMASHIELD PLATINUM Woven Double Velour Vascular Graft01 Branch, Product Code: M00202175834P0 - Product Usage: for use in the replacement or repair of arteries affected with aneury
- Z-1865-2020 · Apr 7, 2020 · TerminatedHEMASHIELD PLATINUM Woven Double Velour Vascular Graft-Angled 4 Branch, Product Code: M00202175730AP0 - Product Usage: for use in the replacement or repair of arteries affected wit
…and 5 more.
Other Graft, Vascular, Synthetic/Biologic Composite devices
- Hemashield M00202166168P0Intervascular Sas · Graft, Vascular, Synthetic/Biologic Composite1 recall3 reports
- Hemashield M002020851890Intervascular Sas · Graft, Vascular, Synthetic/Biologic Composite1 recall2 reports
- Hemashield M002020952070Intervascular Sas · Graft, Vascular, Synthetic/Biologic Composite1 recall0 reports
- Hemashield M00202175928P0Intervascular Sas · Graft, Vascular, Synthetic/Biologic Composite10 reports
- Hemashield M00202175208P0Intervascular Sas · Graft, Vascular, Synthetic/Biologic Composite8 reports
- Hemashield M00202175210P0Intervascular Sas · Graft, Vascular, Synthetic/Biologic Composite8 reports
- AlboGraft Polyester Vascular Graft AMC1407Lemaitre Vascular, Inc. · Graft, Vascular, Synthetic/Biologic Composite6 reports
- Hemashield M00202175430P0Intervascular Sas · Graft, Vascular, Synthetic/Biologic Composite6 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.