Vascular Table without Fowler (USV1) and Ultrasound Vascular Table with Fowler (USV2)
Medical device recall Z-2349-2021. Published in FDA’s Enforcement Report on Sep 1, 2021.
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 Sep 1, 2021. Copied from openFDA on Oct 20, 2026.
- Class II FDA’s class
- Terminated its status, in FDA’s file
- Nationwide FDA’s word for where it went
- 55 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 II, the middle of FDA’s three classes.
“Products that might cause a temporary health problem, or pose only a slight threat of a serious nature. Example: a drug that is under-strength but that is not used to treat life-threatening situations.”
openFDA, in plain words, its enforcement report fields.
“Class II is a situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote.”
FDA’s rule, 21 CFR 7.3(m)(2), eCFR.
What these words mean is quoted from openFDA’s field reference and 21 CFR 7.3.
What’s wrong with it?
Weld failure- the bracket attaches the tabletop tilting actuator to the tabletop frame. If the bracket weld fails, the tabletop tilting action is non-functional
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Which ones are recalled?
Vascular Table without Fowler (USV1) and Ultrasound Vascular Table with Fowler (USV2). Intended Use: Vascular Ultrasound examination table Catalog Number: 66783 and 64219
55 units, in FDA’s words.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Codes to check against yours
Serial Number/Part Number VCF766794 USGNV22723723MTTZZCE2S; VCF767303 USGNV23023723MTTZZ2S; VCF771999 USGNV23023723MTTZZ2S; VCF774252 USGNV23023723MTTZZ2S; VCF776073 USGNV23023723MTTZZ2S; VCF776198 USGNV23023723MTTZZ2S; VCF778246…
Every code shown here, 1,873 characters
Serial Number/Part Number VCF766794 USGNV22723723MTTZZCE2S; VCF767303 USGNV23023723MTTZZ2S; VCF771999 USGNV23023723MTTZZ2S; VCF774252 USGNV23023723MTTZZ2S; VCF776073 USGNV23023723MTTZZ2S; VCF776198 USGNV23023723MTTZZ2S; VCF778246 USGNV23023723MTTZZ2S; VCF778247 USGNV23023723MTTZZ2S; VCF779362 USGNV23023723MTTZZ2S; VCF780260 USGNV23023723MTTZZ2S; VCS781126 USGNV13023723MTTZZ2S; VCF783652 USGNV22723723MTTZZF82S; VCF783969 USGNV23023723MTTZZF82S; VCF785961 USGNV22723723MTTZZCE2S; VCS766698 USGNV12723723MTTZZF62S; VCF768278 USGNV23023723MTTZZCEDRMC2S; VCF770016 USGNV23023723MTTZZ2S; VCF770017 USGNV23023723MTTZZ2S; VCF770571 USGNV23023723MTTZZCE2S; VCF771782 USGNV23023723MTTZZF8MC2S; VCF776974 USGNV22723723MTTZZ2S; VCF778602 USGNV23023723MTTZZ2S; VCF779609 USGNV23023723MTTZZF8CE2S; VCF781198 USGNV23023723MTTZZ2S; VCF784255 USGNV23023723MTTZZCE2S; VCF785376 USGNV23023723MTTZZ2S; VCF785650 USGNV23023723MTTZZF8MC2S; VCF786137 USGNV23023723MTTZZ2S; VCF786173 USGNV23023723MTTZZCE2S; VCF771553 USGNV23023723MTTZZCEMC2S; VCF771554 USGNV23023723MTTZZCEMC2S; VCF785065 USGNV22723723MTTZZF8CEDRDL2S; VCF771992 USGNV23023723MTTZZF8DRDL2S; VCF771993 USGNV23023723MTTZZF8DRDL2S; VCF782916 USGNV23023723MTTZZF8DRDL2S; VCF772035 USGNV22723723MTTZZ2S; VCF777288 USGNV22723723MTTZZ2S; VCF779024 USGNV22723723MTTZZ2S; VCF779025 USGNV22723723MTTZZ2S; VCF779026 USGNV22723723MTTZZ2S; VCF780977 USGNV22723723MTTZZ2S; VCF785219 USGNV22723723MTTZZ2S; VCF771311 USGNV23023723MTTZZ2S; VCF785744 USGNV22723723MTTZZCE2S; VCS772698 USGNV12723723MTTZZ2S; VCF771236 USGNV22723723MTTZZF8CE2S; VCF775658 USGNV23023723MTTZZ2S; VCF776370 USGNV23023723MTTZZ2S; VCF792903 USGNV23023723MTTZZMC2S; VCF773748 USGNV23023723MTTZZF8MC2S; VCF773748 USGNV23023723MTTZZCE2S; VCF779429 USGNV23023723MTTZZF8CE2S; VCF779921 USGNV23023723MTTZZF82S; VCF783233 USGNV23023723MTTZZ2S; VCF786329 USGNV22723723MTTZZ2S;
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.
Nationwide
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.
What these words mean is quoted from openFDA’s field reference and 21 CFR 7.3.
Is it still going on?
Terminated, in FDA’s file.
“FDA has determined that all reasonable efforts have been made to remove or correct the violative product in accordance with the recall strategy, and proper disposition has been made according to the degree of hazard.”
openFDA, on “Terminated”, 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 Jun 29, 2021.
- FDA classified it on Aug 25, 2021.
- FDA’s Enforcement Report published it on Sep 1, 2021.
- FDA terminated it on Oct 5, 2023.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Who is recalling it?
- Oakworks Inc, of New Freedom, PA.
- 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.