Reported Sep 1, 2021 · Terminated

Vascular Table without Fowler (USV1) and Ultrasound Vascular Table with Fowler (USV2). Intended Use: Vascular…

Oakworks Inc.

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: Oakworks Inc · 923 E Wellspring Rd · New Freedom, PA · 17349-8408

Is this the product you have?

  • Vascular Table without Fowler (USV1) and Ultrasound Vascular Table with Fowler (USV2)
  • Intended UseVascular Ultrasound
  • examination table Catalog Number66783 and 64219
Lot codes and dates

55 of 55 products

Products covered by this recall
Model / numberProduct as published
VCF766794Serial Number/ 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
Amount recalled
55 units

Where it was sold

  • Nationwide

Why it was recalled

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

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

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Where this came from

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

Read the FDA (openFDA device enforcement) notice

Notice updated Oct 5, 2023 · Data as of Sep 19, 6:58 PM UTC

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