CLASS II Device recall · Reported 13 May 2020 · FDA Enforcement Report
Hemashield Platinum Woven Double Velour Vascular Graft recalled
Maquet Cardiovascular is recalling Hemashield Platinum Woven Double Velour Vascular Graft- 1 Branch, distributed nationwide in the US. The recall was initiated on 7 Apr 2020 and the FDA has classified it as Class II.
Check your package
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
Recall details
- Recall number
- Z-1870-2020
- FDA event ID
- 85420
- Recalling firm
- Maquet Cardiovascular, Wayne, NJ
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 7 Apr 2020
- FDA classified
- 4 May 2020
- Reported
- 13 May 2020
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Other Reasons
- Device type
- Heart & Vascular Devices
Timeline
| 7 Apr 2020 | Recall initiated by company | |
| 4 May 2020 | Classified by FDA | +27 days |
| 13 May 2020 | Published in enforcement report | +9 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Potential small holes at the seam lines of Hemashield branches causing intra-operative bleeding at the seam lines of the branches of Hemashield grafts
Product as listed by the FDA
HEMASHIELD PLATINUM Woven Double Velour Vascular Graft- 1 Branch, Product Code: M00202175824P0 - Product Usage: for use in the replacement or repair of arteries affected with aneurysmal or occlusive disease.
Where it was distributed
Worldwide distribution - US Nationwide distribution and the countries of Dubai, Argentina, Austria, Belgium, Brazil, Japan, Canada, China, Germany, Spain, Finland, France, UK, Hongkong, Italy, Korea, Netherlands, Poland, Serbia, Sweden.
Questions about this recall
Why was it 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
Which lots are affected?
Serial Numbers: 1069833603 1069800979 1069830915 1069822813 1069826494 1073232852 1073244538 1073248356 1073247694 1073238111 1073244655 1073245805 1074078868 1074096981 1073245180 1075816095 1075833820 1075817616 1075822171 1121372880 1121440106 1121438219 1121372041 1121396486 1121390993 1121413834 1121410287 1123883969 1123881709 1123882605 1126691350 1131379994 1150412103 1150432593 1150316987 1150489896 1150511448 1150483701 1162227315 1162227920 1162231345 1177013851 1176957069 1177022361 1177037106 1177062054 1180553781 1180752802 1184425670 1073247948 1073255445 1075827022 1080534907 1120128533 1120067440 1121368128 1121428442 1121415860 1123880071 1150432730 1150485356 1150485473 1180546087 1184503258 1187865172
Where was it sold?
Worldwide distribution - US Nationwide distribution and the countries of Dubai, Argentina, Austria, Belgium, Brazil, Japan, Canada, China, Germany, Spain, Finland, France, UK, Hongkong, Italy, Korea, Netherlands, Poland, Serbia, Sweden.
What should I do if I have it?
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
Other products in this recall event
23 other products · FDA event 85420This product is part of a recall event; the main page for the event is Hemashield Platinum Woven Double Velour Vascular Graft recalled.
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