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Hemashield M00202175126P0Recalls & reported problems

Intervascular Sas · Hemashield Platinum Woven Straight Double Velour Vascular Graft with Graft Sizer Accessory · Class 2 · Implant

Adverse event reports
3
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00384401018063), received between Jul 17, 2020 and Jan 5, 2023 — classified as 3 malfunctions.

The most frequently reported specific device problem is “Product Quality Problem” (2 reports).

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.

Most reported problems

Device problems

  • Product Quality Problem2
  • Device Damaged Prior to Receipt by User1
  • Nonstandard Device1

Patient problems

  • No Clinical Signs, Symptoms or Conditions2
  • No Patient Involvement1

Recent adverse event reports

The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.

  • MalfunctionJan 5, 2023Nonstandard Device; Product Quality Problem; Nonstandard Device; Product Quality Problem

    COMPLAINT #(B)(4).

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 16103058 ↗
  • MalfunctionOct 11, 2022Product Quality Problem; Product Quality Problem

    IT WAS REPORTED TO INTERVASCULAR THAT WHEN THE DOCTOR OPENED THE PRODUCT, HE FOUND THERE WERE SOME YELLOW SPOTS ON THE SURFACE OF THE GRAFT. HE CHANGE ANOTHER GRAFT INSTEAD. THE EVENT OCCURED PRIOR TO USE, THE SURGERY WAS NOT DELAYED AND NO HAZARD ISSUE OCCURRED. COMPLAINT # (B)(4).

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 15575941 ↗
  • MalfunctionJul 17, 2020Device Damaged Prior to Receipt by User; Device Damaged Prior to Receipt by User

    SEE INITIAL MFR REPORT # 1640201-2020-00017. COMPLAINT # (B)(4).

    Patient problems: No Patient Involvement

    MAUDE report 10289442 ↗

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-1866-2020 · Apr 7, 2020 · Terminated
    HEMASHIELD PLATINUM Woven Double Velour Vascular Graft-4 Branch, Product Code: M00202175732P0 - Product Usage: for use in the replacement or repair of arteries affected with aneury
  • Z-1867-2020 · Apr 7, 2020 · Terminated
    HEMASHIELD 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-1876-2020 · Apr 7, 2020 · Terminated
    HEMASHIELD 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-1873-2020 · Apr 7, 2020 · Terminated
    HEMASHIELD PLATINUM Woven Double Velour Vascular Graft- 1 Branch, Product Code: M00202175830P0 - Product Usage: for use in the replacement or repair of arteries affected with aneur
  • Z-1874-2020 · Apr 7, 2020 · Terminated
    HEMASHIELD 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-1869-2020 · Apr 7, 2020 · Terminated
    HEMASHIELD 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-1875-2020 · Apr 7, 2020 · Terminated
    HEMASHIELD 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-1868-2020 · Apr 7, 2020 · Terminated
    HEMASHIELD 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-1865-2020 · Apr 7, 2020 · Terminated
    HEMASHIELD 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
  • Z-1881-2020 · Apr 7, 2020 · Terminated
    HEMASHIELD 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-1878-2020 · Apr 7, 2020 · Terminated
    HEMASHIELD 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-1880-2020 · Apr 7, 2020 · Terminated
    HEMASHIELD 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-1879-2020 · Apr 7, 2020 · Terminated
    HEMASHIELD 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-1877-2020 · Apr 7, 2020 · Terminated
    HEMASHIELD 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-1871-2020 · Apr 7, 2020 · Terminated
    HEMASHIELD PLATINUM Woven Double Velour Vascular Graft-1 Branch, Product Code: M00202175826P0 - Product Usage: for use in the replacement or repair of arteries affected with aneury

…and 5 more.

Other Graft, Vascular, Synthetic/Biologic Composite devices

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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.