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Hemashield M002020851690Recalls & reported problems

Intervascular Sas · Hemashield Gold Knitted Microvel Bifurcated Double Velour Vascular Graft with Graft Sizer Accessory · Class 2 · Implant

Adverse event reports
1
Deaths reported
0
Injuries reported
1
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00384401017738), received between Jul 11, 2016 and Jul 11, 2016 — classified as 1 injury.

The most frequently reported specific device problem is “Manufacturing, Packaging or Shipping Problem” (1 report).

6 other recalls cover devices cleared under the same FDA submission (K954848); 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

  • Manufacturing, Packaging or Shipping Problem1

Patient problems

  • Blood Loss1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • InjuryJul 11, 2016Manufacturing, Packaging or Shipping Problem; Manufacturing, Packaging or Shipping Problem

    DURING AN ABDOMINAL ANEURYSM SURGERY PERFORMED ON (B)(6) 2016, BLOOD LEAK WAS NOTED FROM THE BIFURCATION OF THE MAIN GRAFT SEGMENT. ASTRICTION AND GAUZE APPLICATION WERE PERFORMED TO STOP THE BLEEDING. THE BLEEDING WAS FINALLY STOPPED BY ADMINISTRATION OF PROTAMINE. THE GRAFT REMAINED IMPLANTED, WITHOUT ANY ADVERSE OUTCOME FOR THE PATIENT.

    Patient problems: Blood Loss

    MAUDE report 5781625 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K954848. One submission often covers many models, so check the product and lot details in each record.

  • Z-0729-2022 · Jan 14, 2022 · Terminated
    HEMASHIELD GOLD KNITTED MICROVEL DOUBLE VELOUR VASCULAR GRAFT- D: 7 mm; L: 60 cm Indicated for use in the replacement or repair of arteries affected with aneurysmal or occlusive
  • Z-0403-2022 · Dec 1, 2021 · Terminated
    Hemashield Gold Knitted Bifurcated, 18 mm x 9 mm; reference number M002020851890
  • Z-1861-2020 · Apr 7, 2020 · Terminated
    Hemashield Gold Knitted Microvel Double Velour Vascular Graft Axillo-bifemoral, Product Code: M002020955890 - Product Usage: for use in the replacement or repair of arteries affect
  • Z-1859-2020 · Apr 7, 2020 · Terminated
    Hemashield Gold Knitted Microvel Double Velour Vascular Graft-Axillo-bifemoral, Product Code: M002020955010 - Product Usage: For use in the replacement or repair of arteries affect
  • Z-1860-2020 · Apr 7, 2020 · Terminated
    Hemashield Gold Knitted Microvel Double Velour Vascular Graft-Axillo-bifemoral, Product Code: M002020955880 - Product Usage: for use in the replacement or repair of arteries affect
  • Z-2066-2010 · May 24, 2010 · Terminated
    Hemashield Gold Woven and Knitted Double Vascular Grafts.

Other Graft, Vascular, Synthetic/Biologic Composite devices

All Graft, Vascular, Synthetic/Biologic Composite devices →

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