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Hemashield M00202175128P0Recalls & reported problems

Intervascular Sas · Hemashield Platinum Woven Straight 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 00384401018070), received between Feb 6, 2018 and Oct 14, 2021 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Device Damaged Prior to Use” (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.

Most reported problems

Device problems

  • Device Damaged Prior to Use1
  • Incomplete or Missing Packaging1

Patient problems

  • No Clinical Signs, Symptoms or Conditions1
  • Not Applicable1

Recent adverse event reports

The 2 most recent of 2 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 12631884 ↗
  • MalfunctionFeb 6, 2018Incomplete or Missing Packaging; Incomplete or Missing Packaging

    IT WAS REPORTED BY THE HOSPITAL TWO CASES WERE THE DEVICES WERE FOUND WITH NO LABEL FOR DOCUMENTATION AND NO DIRECTION FOR USE IN THE PACKAGING. THE DEVICES WERE USED WITHOUT ANY CONSEQUENCE FOR PATIENTS. THE SECOND CASE IS SUBMITTED UNDER MANUFACTURER REPORT NUMBER 1640201-2018-00004.

    Patient problems: Not Applicable

    MAUDE report 7243486 ↗

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-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-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-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-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
  • 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-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-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-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-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-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-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-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-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-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-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

…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.