Oakworks Recalls
9 recalls on record · March 7, 2018 to January 24, 2024 · Medical Devices
Recalls by year
18
19
21
22
24
Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
January 24, 2024Medical DevicesFDA
Oakworks Inc recalls Ultrasound EA (Ergonomic Advantage) table version; V2 (Vascular 2 Section) Echocardiography -An Ultrasound examination t
Hazard: Backrest platform stress fracture - the table is not operational in an inclined position
January 24, 2024Medical DevicesFDA
Oakworks Inc recalls Ultrasound EA (Ergonomic Advantage) table versions; G3 Multi-Specialty Echocardiography and Multi-Specialty with Electri
Hazard: Backrest platform stress fracture - the table is not operational in an inclined position
January 24, 2024Medical DevicesFDA
Oakworks Inc recalls Ultrasound EA (Ergonomic Advantage) table versions; G3 (General 3 Section) Echocardiography -An Ultrasound examination t
Hazard: Backrest platform stress fracture - the table is not operational in an inclined position
January 24, 2024Medical DevicesFDA
Oakworks Inc recalls Ultrasound EA (Ergonomic Advantage) table versions; G2 (GENERAL 2) -An Ultrasound examination table
Hazard: Backrest platform stress fracture - the table is not operational in an inclined position
June 15, 2022Medical DevicesFDA
Oakworks Inc recalls Oakworks Bed (Emergency Field Bed); Model No. OBMPBR361980A6TTGRCS
Hazard: The warning label was printed with the incorrect weight capacity. The correct weight limit is 400 lbs., but the label states 500 lbs.
June 15, 2022Medical DevicesFDA
Oakworks Inc recalls PX200 Emergency Relief Bed; Model No. PXEXEB362280A6TTZZH4C19
Hazard: Product label was printed without the UDI number and warning label was printed with the incorrect weight capacity. The correct weight limit is 400 lbs., but the label states 500 lbs.
September 1, 2021Medical DevicesFDA
Oakworks Inc recalls Vascular Table without Fowler (USV1) and Ultrasound Vascular Table with Fowler (USV2). Intended Use: Vascular Ultrasound
Hazard: 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
May 29, 2019Medical DevicesFDA
Oakworks Inc recalls OAKWORKS Inc.Lithotripsy/Urology Table: CFLU401, Catalog Number: 75216-T01 - Product Usage: Oakworks¿ Imaging Tables are
Hazard: Table assembly error with incorrect actuators for the lateral and longitudinal table movements
March 7, 2018Medical DevicesFDA
Oakworks Inc recalls Foot Controls impacted for the following devices: OAKWORKS¿ Medical CFPM 300 Imaging Table OAKWORKS¿ Medical CFPM 30
Hazard: The foot control used on the OAKWORKS¿ Inc., CFPM300, CFPM301, CFPM400, CFPM401, CFPMB301, CFUR301, CFUR401 and CFLU401 Imaging Tables can become lodged under the base or under the column of the table.