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Hemashield M00202175134P0Recalls & 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 00384401018100), received between Jul 17, 2020 and Oct 14, 2021 — classified as 3 malfunctions.

The most frequently reported specific device problem is “Device Damaged Prior to Receipt by User” (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

  • Device Damaged Prior to Receipt by User2
  • Device Damaged Prior to Use1

Patient problems

  • No Patient Involvement2
  • No Clinical Signs, Symptoms or Conditions1

Recent adverse event reports

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

  • MalfunctionOct 14, 2021Device Damaged Prior to Use; Device Damaged Prior to Use

    THIS MDR IS PART OF A SERIES OF 2 COMPLAINTS INVOLVING 2 PRODUCTS DELIVERED IN SAME PARCEL AND RELATED TO A SINGLE EVENT. BOTH PRODUCTS WERE DELIVERED DAMAGED, AS THE INNER PACKING WAS CRUSHED. COMPLAINT : #(B)(4).

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 12631879 ↗
  • MalfunctionJul 17, 2020Device Damaged Prior to Receipt by User; Device Damaged Prior to Receipt by User

    SEE INITIAL MFR REPORT # 1640201-2020-00014. COMPLAINT # (B)(4).

    Patient problems: No Patient Involvement

    MAUDE report 10289437 ↗
  • MalfunctionJul 17, 2020Device Damaged Prior to Receipt by User; Device Damaged Prior to Receipt by User

    SEE INITIAL MFR REPORT # 1640201-2020-00015. COMPLAINT # (B)(4).

    Patient problems: No Patient Involvement

    MAUDE report 10289428 ↗

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-1864-2020 · Apr 7, 2020 · Terminated
    HEMASHIELD 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-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-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-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-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-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-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-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-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-1882-2020 · Apr 7, 2020 · Terminated
    HEMASHIELD 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-1870-2020 · Apr 7, 2020 · Terminated
    HEMASHIELD 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-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-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-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

…and 5 more.

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