Manufacturer

Oakworks Inc

9 recalls in our database name Oakworks Inc as the manufacturing or recalling firm.

What the numbers show

Total: 9
Critical: 0
Severe: 0
Most recent: 2024-01-24

Of the 9 recalls from Oakworks Inc we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 0 (0%) are Severe.

About this listing

The manufacturer string comes from the agency’s own source notice — for FDA recalls, the “recalling firm” field; for NHTSA recalls, the vehicle manufacturer; for CPSC recalls, the firm-of-record on the joint press release. A single corporate family can appear under multiple manufacturer strings as agency notices aren’t standardized on a canonical name. If you don’t see recalls you expect, try a parent-company search or a broader full-text search.

Severity scores below are computed from the agency’s classification and the recall text, never from manufacturer behaviour or history. Many manufacturers issue routine corrective actions (software updates, labelling corrections) that are correctly scored low — having recalls on this list isn’t inherently a quality signal.

1–9 of 9

HighFDA (Devices)·Z-0729-2024·2024-01-24
Ultrasound examination tables recalled for backrest platform stress fractures
Oakworks recalled 20 Ultrasound EA and G3 examination tables due to backrest platform stress fractures that prevent proper operation in inclined positions. Affected units are identified by serial number.
Product
Ultrasound EA (Ergonomic Advantage) table versions; G3 Multi-Specialty Echocardiography and Multi-Specialty with Electric Access Back Supports [left & right}
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0730-2024·2024-01-24
Ultrasound Examination Table Recalled for Backrest Stress Fracture
Oakworks Inc is recalling 28 Ultrasound EA examination tables due to backrest platform stress fractures that prevent operation in an inclined position.
Product
Ultrasound EA (Ergonomic Advantage) table version; V2 (Vascular 2 Section) Echocardiography -An Ultrasound examination table
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0728-2024·2024-01-24
Ultrasound Examination Table Recall Due to Backrest Platform Stress Fracture
Oakworks Inc is recalling Ultrasound EA examination tables because the backrest platform can develop stress fractures, making the table inoperable in inclined positions. Approximately 104 units distributed nationwide are affected.
Product
Ultrasound EA (Ergonomic Advantage) table versions; G3 (General 3 Section) Echocardiography -An Ultrasound examination table
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0727-2024·2024-01-24
Ultrasound examination table recalled due to backrest platform stress fracture
Oakworks Inc is recalling 212 Ultrasound EA G2 examination tables nationwide due to stress fractures in the backrest platform that make the equipment non-operational in an inclined position.
Product
Ultrasound EA (Ergonomic Advantage) table versions; G2 (GENERAL 2) -An Ultrasound examination table
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1238-2022·2022-06-15
Emergency relief bed recalled for missing UDI and incorrect weight limit label
Oakworks Inc is recalling PX200 Emergency Relief Beds due to labeling defects. The product label is missing the UDI number and states an incorrect weight capacity of 500 lbs instead of the actual 400 lb limit.
Product
PX200 Emergency Relief Bed; Model No. PXEXEB362280A6TTZZH4C19
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1239-2022·2022-06-15
Oakworks Emergency Field Bed Recalled for Incorrect Weight Capacity Label
Oakworks has recalled 109 units of its Emergency Field Bed due to an incorrect weight capacity label. The label states 500 lbs, but the bed's actual weight limit is 400 lbs.
Product
Oakworks Bed (Emergency Field Bed); Model No. OBMPBR361980A6TTGRCS
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2349-2021·2021-09-01
Vascular Ultrasound Examination Table Recalled for Weld Failure
Oakworks vascular ultrasound examination tables (models USV1 and USV2) are recalled due to potential weld failure in the tilting mechanism bracket. A failed weld could prevent the table from tilting, affecting patient positioning.
Product
Vascular Table without Fowler (USV1) and Ultrasound Vascular Table with Fowler (USV2). Intended Use: Vascular Ultrasound examination table Catalog Number: 66783 and 64219
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1411-2019·2019-05-29
Oakworks Lithotripsy Table Recalled for Incorrect Actuator Assembly Error
Oakworks Inc. is recalling three Lithotripsy/Urology Tables due to an assembly error involving incorrect actuators for lateral and longitudinal movements.
Product
OAKWORKS Inc.Lithotripsy/Urology Table: CFLU401, Catalog Number: 75216-T01 - Product Usage: Oakworks¿ Imaging Tables are radiographic tables intended for use with mobile or compact stationary C-arm Imaging Systems. It is ideally suited for pain management imaging and therapeutic
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0703-2018·2018-03-07
Oakworks Medical Imaging Table Foot Controls Recalled for Lodging Hazard
Oakworks Inc. is recalling foot controls for specific medical imaging tables because they can become lodged under the table base or column.
Product
Foot Controls impacted for the following devices: OAKWORKS¿ Medical CFPM 300 Imaging Table OAKWORKS¿ Medical CFPM 301 Imaging Table OAKWORKS¿ Medical CFPM 400 Imaging Table OAKWORKS¿ Medical CFPM 401 Imaging Table OAKWORKS¿ Medical CFPMB 301 Bariatric Imaging Table OAKWOR
Category
Medical Device
Distribution
Distributed nationwide