Hemashield M00202175426P0Recalls & reported problems
Intervascular Sas · Hemashield Platinum Woven Straight Double Velour Vascular Graft with Graft Sizer Accessory · Class 2 · Implant
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00384401018230), received between Oct 7, 2022 and Oct 7, 2022 — classified as 1 malfunction.
The most frequently reported specific device problem is “Product Quality Problem” (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
- Product Quality Problem1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionOct 7, 2022Product Quality Problem; Product Quality Problem
IT WAS REPORTING TO INTERVASCULAR THAT WHILE PREPARING FOR THE AORTIC DISSECTION SURGERY, A DISCOLORED AREA WAS DISCOVERED WITH MELTED COLLAGEN IN THE PRODUCT. THE OPERATION WAS COMPLETED WITH ANOTHER PRODUCT OF THE SAME MODEL STOCKED IN THE HOSPITAL. COMPLAINT #: (B)(4). PLEASE NOTE THAT THIS COMPLAINT IS ONE OF A SERIES OF TWO COMPLAINTS, THE SECOND COMPLAINT #: (B)(4) IS ALSO THE SUBJECT OF AN INITIAL EMDR REPORTING.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15560161 ↗
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-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-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-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-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-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-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-1871-2020 · Apr 7, 2020 · TerminatedHEMASHIELD 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-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
- Z-1873-2020 · Apr 7, 2020 · TerminatedHEMASHIELD 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-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-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-1866-2020 · Apr 7, 2020 · TerminatedHEMASHIELD 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-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
…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.