Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 13, 2026, FDA's public records list Oakworks with 9 device recalls. The most recent is a device recall dated Dec 5, 2023: Ultrasound EA (Ergonomic Advantage) table versions; G3 Multi-Specialty Echocardiography ….
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
A hatched bar is a year that is not over, so its count covers only part of the year.
| Date | Record | Source |
|---|---|---|
| Dec 5, 2023 | Ultrasound EA (Ergonomic Advantage) table versions; G3 Multi-Specialty Echocardiography and Multi-Specialty with Electric Access Back SupporClass II · Backrest platform stress fracture - the table is not operational in an inclined position | Device recalls |
| Dec 5, 2023 | Ultrasound EA (Ergonomic Advantage) table versions; G3 (General 3 Section) Echocardiography -An Ultrasound examination tableClass II · Backrest platform stress fracture - the table is not operational in an inclined position | Device recalls |
| Dec 5, 2023 | Ultrasound EA (Ergonomic Advantage) table version; V2 (Vascular 2 Section) Echocardiography -An Ultrasound examination tableClass II · Backrest platform stress fracture - the table is not operational in an inclined position | Device recalls |
| Dec 5, 2023 | Ultrasound EA (Ergonomic Advantage) table versions; G2 (GENERAL 2) -An Ultrasound examination tableClass II · Backrest platform stress fracture - the table is not operational in an inclined position | Device recalls |
| Apr 21, 2022 | PX200 Emergency Relief Bed; Model No. PXEXEB362280A6TTZZH4C19Class II · Product label was printed without the UDI number and warning label was printed with the incorrect weight capacity. The c | Device recalls |
| Apr 21, 2022 | Oakworks Bed (Emergency Field Bed); Model No. OBMPBR361980A6TTGRCSClass II · The warning label was printed with the incorrect weight capacity. The correct weight limit is 400 lbs., but the label st | Device recalls |
| Jun 29, 2021 | Vascular Table without Fowler (USV1) and Ultrasound Vascular Table with Fowler (USV2). Intended Use: Vascular Ultrasound examination table CClass II · Weld failure- the bracket attaches the tabletop tilting actuator to the tabletop frame. If the bracket weld fails, the t | Device recalls |
| May 2, 2019 | OAKWORKS Inc.Lithotripsy/Urology Table: CFLU401, Catalog Number: 75216-T01 - Product Usage: Oakworks¿ Imaging Tables are radiographic tablesClass II · Table assembly error with incorrect actuators for the lateral and longitudinal table movements | Device recalls |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
