VasoView HemoPro Endoscopic Vessel Harvesting System
Medical device recall Z-0092-2025. Published in FDA’s Enforcement Report on Nov 6, 2024.
- FDA Class I
No Watch here, and no alerts: openFDA asks that its enforcement data “should not be used as a method to collect data to issue alerts to the public, nor should it be used to track the lifecycle of a recall” (openFDA). For FDA’s own recall emails, subscribe at FDA. FDA’s own record is on accessdata.fda.gov.
The short answer
Published in FDA’s Enforcement Report on Nov 6, 2024. Copied from openFDA on Oct 20, 2026.
- Class I FDA’s most serious class (needs attention)
- Ongoing its status, in FDA’s file
- Nationwide FDA’s word for where it went
- 28,809 units how much, in FDA’s words
Every line below is in FDA’s own words, with its source beside it. FDA’s terms are explained in FDA’s own words.
How serious is it, by FDA’s class?
Class I, the most serious of FDA’s three classes.
“Dangerous or defective products that predictably could cause serious health problems or death. Examples include: food found to contain botulinum toxin, food with undeclared allergens, a label mix-up on a lifesaving drug, or a defective artificial heart valve.”
openFDA, in plain words, its enforcement report fields.
“Class I is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.”
FDA’s rule, 21 CFR 7.3(m)(1), eCFR.
What these words mean is quoted from openFDA’s field reference and 21 CFR 7.3.
What’s wrong with it?
There were reports of the silicone detaching from the Jaws of the Harvesting Tool during use.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Which ones are recalled?
VasoView HemoPro Endoscopic Vessel Harvesting System, Product Codes VH-3000-W and VH-3500
28,809 units, in FDA’s words.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Codes to check against yours
UDI-DI: VH-3000-W - 00607567700413, VH-3500 - 00607567701250; Lot Numbers: VH-3000-W: 3000365379, 3000382334, 3000392749; VH-3500: 3000333967 3000354228 3000364520 3000376542 3000384902 3000400713 3000339701 3000355224 3000365391…
Every code shown here, 1,340 characters
UDI-DI: VH-3000-W - 00607567700413, VH-3500 - 00607567701250; Lot Numbers: VH-3000-W: 3000365379, 3000382334, 3000392749; VH-3500: 3000333967 3000354228 3000364520 3000376542 3000384902 3000400713 3000339701 3000355224 3000365391 3000376883 3000385174 3000401094 3000340534 3000355369 3000366446 3000377320 3000385849 3000401623 3000341133 3000355798 3000366831 3000377699 3000386206 3000402378 3000341675 3000356048 3000367160 3000378079 3000386871 3000403161 3000342250 3000357837 3000367439 3000378654 3000387986 3000403837 3000342251 3000360574 3000367542 3000379282 3000387987 3000404029 3000343264 3000360576 3000367852 3000379691 3000388401 3000404374 3000343266 3000360775 3000368165 3000380264 3000388676 3000404720 3000344887 3000361036 3000368658 3000380475 3000389329 3000411951 3000345068 3000361423 3000369005 3000380671 3000392530 3000346640 3000361707 3000369122 3000381049 3000392531 3000351187 3000362064 3000369645 3000381287 3000393159 3000351376 3000362258 3000370069 3000381620 3000393427 3000351407 3000362671 3000370290 3000382054 3000393838 3000351619 3000362933 3000372257 3000382868 3000394234 3000351747 3000363162 3000375534 3000383367 3000395128 3000351860 3000363947 3000375776 3000383779 3000398856 3000352770 3000364082 3000376132 3000384088 3000399341 3000354226 3000364309 3000376388 3000384382 3000399911
Copied exactly as FDA lists them: lot and serial numbers, dates and other codes on the product or its label.
Where did it go?
FDA’s words for the “general area of initial distribution”: where the firm first shipped it.
Worldwide distribution. US Nationwide. Brazil, China, and Hong Kong.
These words name no state.
What FDA means by nationwide
“The term “nationwide” is defined to mean the fifty states or a significant portion. Note that subsequent distribution by the consignees to other parties may not be included.”
openFDA, its enforcement report fields.
The words say it went outside the United States too.
What these words mean is quoted from openFDA’s field reference and 21 CFR 7.3.
Is it still going on?
Ongoing, in FDA’s file.
“A recall which is currently in progress.”
openFDA, on “On-Going”, its enforcement report fields.
What these words mean is quoted from openFDA’s field reference and 21 CFR 7.3.
- The firm began the recall on Sep 20, 2024.
- FDA classified it on Oct 25, 2024.
- FDA’s Enforcement Report published it on Nov 6, 2024.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Who is recalling it?
- Maquet Cardiovascular, LLC, of Wayne, NJ.
- Who began it, in FDA’s words: Voluntary: Firm initiated.
- How the firm first told its customers: Letter.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
What this record can’t tell you
- Whether your own one is affected: compare the codes, dates and numbers above with yours. When unsure, ask the firm or the store.
- Where it went after the firm’s first shipments. FDA’s words cover the firm’s initial distribution, and, in FDA’s words, “subsequent distribution by the consignees to other parties may not be included.”
- How many have been returned, corrected or destroyed: FDA’s report doesn’t say.
- Whether anyone was hurt or fell ill: the report doesn’t say.
- How current it is: openFDA publishes FDA’s Enforcement Report weekly, after FDA does, and a firm can announce a recall weeks before it appears there. openFDA’s own caution: “This data should not be used as a method to collect data to issue alerts to the public, nor should it be used to track the lifecycle of a recall.”
- A product with no recall here isn’t safe by that: FDA’s report lists the recalls FDA classified, and when.
Hearth Record wrote these lines; the quotations are FDA’s.
Sources
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U.S. Food and Drug Administration, Device recall enforcement reports.
Released Oct 14, 2026 and checked Oct 20, 2026. Updated weekly. Public domain (CC0 1.0, openFDA). FDA asks that nothing suggest it endorses this site.
Recalls of food, medicines, medical devices, pet food and animal drugs are from the U.S. Food and Drug Administration (FDA). FDA does not endorse Hearth Record. openFDA: “Do not rely on openFDA to make decisions regarding medical care.” Copied on Oct 20, 2026.