RecallRadar

FDA Device recall Z-1879-2020

HEMASHIELD PLATINUM Woven Double Velour Vascular Graft-4 Branch, Product Code: M00202175924P0 - Product Usage: for use in the replacement o…

On 2020-05-13 the FDA classified a Class II recall of HEMASHIELD PLATINUM Woven Double Velour Vascular Graft-4 Branch, Product Code: M00202175924P0 - Product Usage: for use in the replacement o… by Maquet Cardiovascular, citing potential small holes at the seam lines of Hemashield branches causing intra-operative bleeding at the seam lines of the branches of Hemashield grafts.

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-1879-2020
ClassificationClass II
Statusterminated
Initiated2020-04-07
Published2020-05-13
Last updated2026-09-13 11:55 UTC
CompanyMaquet Cardiovascular
DistributionUS

Product

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 aneurysmal or occlusive disease.

Reason

Potential small holes at the seam lines of Hemashield branches causing intra-operative bleeding at the seam lines of the branches of Hemashield grafts

Identifiers

code_info
Serial Numbers: 1130028529 1138737382 1151582817 1151580283 1153694149 1158765278 1165139009 1165161757 1165201073 11…Serial Numbers: 1130028529 1138737382 1151582817 1151580283 1153694149 1158765278 1165139009 1165161757 1165201073 1165174827 1165129349 1165209939 1165131353 1165124986 1180826106 1138872368 1153712022 1157288202 1158765044 1165159382

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1879-2020%22

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