The Recall Desk
HighFDA (Devices)·Z-1869-2020·Announced 2020-05-13

Maquet Hemashield Platinum Vascular Grafts Recalled for Seam Defects

Maquet is recalling Hemashield Platinum vascular grafts due to potential small holes at seam lines that may cause intra-operative bleeding.

What this means for you

Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.

Our severity reasoning: The recall involves a medical device with a defect that poses a risk of harm (intra-operative bleeding) but does not report confirmed injuries or deaths, fitting the 'High' severity criteria for risk-of-harm products where injury has not yet been reported.

Plain-English summary

Maquet Cardiovascular, LLC is recalling specific units of the HEMASHIELD PLATINUM Woven Double Velour Vascular Graft- 1 Branch. The recall is issued because of potential small holes at the seam lines of the graft branches, which could cause intra-operative bleeding during surgery.

The affected product is used for the replacement or repair of arteries affected with aneurysmal or occlusive disease. The recall includes specific serial numbers listed in the official notice. Distribution was worldwide, including the United States and various international locations.

Healthcare providers and patients should contact Maquet Cardiovascular for further instructions regarding the affected devices. No specific dates or unit counts are provided in the source text.

The recalled product

Product
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 aneurysmal or occlusive disease.

Distribution

Distributed nationwide across the United States.

Part of a larger recall action

This product is one of 24 recalled by Maquet Cardiovascular, LLC under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.

See all 24 products in this recall →