Reported May 13, 2020 · Terminated

HEMASHIELD PLATINUM Woven Double Velour Vascular Graft-1 Branch, Product Code: M00202175826P0 - Product Usage: for use…

Maquet Cardiovascular, LLC

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Maquet Cardiovascular, LLC · 45 Barbour Pond Dr · Wayne, NJ · 07470-2094

Is this the product you have?

  • HEMASHIELD PLATINUM Woven Double Velour Vascular Graft-1 Branch
  • Product CodeM00202175826P0 -
  • Product Usagefor use in the replacement or repair of arteries affected with aneurysmal or occlusive disease
Lot codes and dates
  • Serial Numbers

    79 of 79 codes

    • 1070172386
    • 1070172035
    • 1070165805
    • 1070170614
    • 1069855417
    • 1070722490
    • 1070716317
    • 1070692463
    • 1070716668
    • 1073219687
    • 1073220795
    • 1073223015
    • 1074236324
    • 1073239612
    • 1074517570
    • 1079999309
    • 1079997985
    • 1080000259
    • 1080547235
    • 1080509568
    • 1080566478
    • 1080564686
    • 1108346226
    • 1111646683
    • 1111648592
    • 1111705379
    • 1111680044
    • 1111803731
    • 1111646078
    • 1111719462
    • 1115868785
    • 1117833189
    • 1117882017
    • 1117871578
    • 1117912903
    • 1117878104
    • 1117848422
    • 1117847877
    • 1118870707
    • 1118858809
    • 1118864514
    • 1146813425
    • 1146795181
    • 1146785287
    • 1146815568
    • 1150324250
    • 1150260235
    • 1150306859
    • 1150311668
    • 1150308046
    • 1150468978
    • 1150337808
    • 1150339112
    • 1150343747
    • 1170653063
    • 1170656610
    • 1170622485
    • 1170679066
    • 1177871479
    • 1177878356
Amount recalled
N/A

This recall covers 24 products

The agency filed one notice per product. You are reading one of them; the other 23 are below.

11 more are in the archive.

Where it was sold

  • Nationwide

Why it was recalled

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

This product could cause temporary or reversible health problems — stop using it.

Want the full recall guide?

The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Notice updated Nov 5, 2021 · Data as of Sep 19, 4:49 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.