Reported May 13, 2020 · Terminated

HEMASHIELD PLATINUM Woven Double Velour Vascular Graft- 1 Branch, Product Code: M00202175830P0 - 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 CodeM00202175830P0 -
  • Product Usagefor use in the replacement or repair of arteries affected with aneurysmal or occlusive disease
Lot codes and dates
  • Serial Numbers

    150 of 150 codes

    • 1069844373
    • 1069859235
    • 1070838372
    • 1070706306
    • 1070885876
    • 1070696535
    • 1070880206
    • 1070698932
    • 1070693359
    • 1070875260
    • 1070859895
    • 1071599689
    • 1071623404
    • 1071635929
    • 1071640855
    • 1071595383
    • 1072244650
    • 1072221218
    • 1072235164
    • 1073312349
    • 1074236187
    • 1074521366
    • 1075883407
    • 1076662460
    • 1076662089
    • 1076657163
    • 1076657651
    • 1077516221
    • 1077516455
    • 1077512637
    • 1077509366
    • 1077515793
    • 1077506795
    • 1077514292
    • 1077510006
    • 1077509132
    • 1080021177
    • 1080028425
    • 1080022190
    • 1080038065
    • 1080016505
    • 1080020047
    • 1080020906
    • 1080022444
    • 1080034247
    • 1080026145
    • 1107350739
    • 1107370878
    • 1107397055
    • 1107542300
    • 1107356954
    • 1107534803
    • 1111727076
    • 1111767628
    • 1111828116
    • 1111802952
    • 1111831484
    • 1111976640
    • 1111962791
    • 1111974477
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, 4:54 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.