Oakworks Inc recalls
Every recall we track for Oakworks Inc — 9 in all, from 2017–2023 — plus the complaints and injury reports the public filed about them. 2 are rated “stop using now”.
Recalls per year, by danger level
Recalls from Oakworks Inc peaked in 2023 (4); 9 since 2017. 22% rated “stop using now”.
All FDA recall records for Oakworks Inc since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 1 | 0 | 0 | 1 |
| 2018 | 0 | 0 | 0 | 0 | 0 |
| 2019 | 0 | 1 | 0 | 0 | 1 |
| 2020 | 0 | 0 | 0 | 0 | 0 |
| 2021 | 0 | 1 | 0 | 0 | 1 |
| 2022 | 0 | 0 | 2 | 0 | 2 |
| 2023 | 2 | 2 | 0 | 0 | 4 |
| 2024 | 0 | 0 | 0 | 0 | 0 |
| 2025 | 0 | 0 | 0 | 0 | 0 |
| 2026 (to date) | 0 | 0 | 0 | 0 | 0 |
What to do if you have a recalled Oakworks Inc product
- Match the model, catalog or lot number on your device to the recall.
- Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
- Report problems to FDA MedWatch.
All Oakworks Inc recalls
5 shown- Use cautionMedical device
Oakworks Inc recalls Ultrasound EA (Ergonomic Advantage) table versions; G3 Multi-Specialty Echocardiography and Multi-Specialty with
Oakworks recalls Ultrasound EA and G3 Multi-Specialty Echocardiography tables due to backrest platform stress fractures when inclined. Affected units have specific serial numbers and UDI codes.
OakworksDec 5, 2023 - Lower riskMedical device
Oakworks Inc recalls PX200 Emergency Relief Bed; Model No. PXEXEB362280A6TTZZH4C19
Oakworks recalls PX200 Emergency Relief Beds with incorrect weight capacity labels (stating 500 lbs when it should be 400 lbs). Affected units have specific serial numbers. Contact Oakworks for replacement.
OakworksApr 21, 2022 - Use cautionMedical device
Oakworks Inc recalls Vascular Table without Fowler (USV1) and Ultrasound Vascular Table with Fowler (USV2). Intended Use: Vascular
Oakworks recalls two ultrasound vascular tables (USV1 and USV2) due to potential weld failure in the tabletop tilting actuator bracket. This could prevent proper table tilting during medical procedures. Affected units have specific serial numbers.
OakworksJun 29, 2021 - Use cautionMedical device
Oakworks Inc recalls OAKWORKS Inc.Lithotripsy/Urology Table: CFLU401, Catalog Number: 75216-T01 - Product Usage: Oakworks¿ Imaging Tables
Oakworks recalls specific lithotripsy/urology tables with assembly errors that could cause injury during use. Affected models include CFLU401 with serial numbers FLL745088-90. Contact Oakworks for details.
OakworksMay 2, 2019 - Use cautionMedical device
Oakworks Inc recalls Foot Controls impacted for the following devices: OAKWORKS¿ Medical CFPM 300 Imaging Table OAKWORKS¿ Medical CFPM 301
Oakworks recalls medical imaging tables with foot controls that can become lodged under the table base or column, posing a risk of injury during use. Affected models include CFPM 300, CFPM 301, and others. Consumers should check their table model and contact Oakworks for details.
OakworksJul 31, 2017
Oakworks Inc recall questions
How many recalls has Oakworks Inc had?
9 recalls from Oakworks Inc are on record with U.S. safety agencies, from 2017–2023.
What is the most recent Oakworks Inc recall?
Oakworks Inc recalls Ultrasound EA (Ergonomic Advantage) table versions; G3 Multi-Specialty Echocardiography and Multi-Specialty with, dated Dec 5, 2023. Every Oakworks Inc recall is listed on this page, newest first.
What should I do if I have a recalled Oakworks Inc product?
Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.
How do I get alerts for new Oakworks Inc recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.