courtlistener_docket
1 records
Speights v. Oakworks, Inc.
2026-04-01
Federal docket 1:26-cv-00838 (pamd); matched party 'Oakworks, Inc.'
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fda
5 records
FDA Device Recall: Ultrasound EA (Ergonomic Advantage) table versions; G3 Multi-Specialty Echocardi
2024-01-24
Class II — Backrest platform stress fracture - the table is not operational in an inclined position
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FDA Device Recall: PX200 Emergency Relief Bed; Model No. PXEXEB362280A6TTZZH4C19
2022-06-15
Class II — 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.
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FDA Device Recall: Oakworks Bed (Emergency Field Bed); Model No. OBMPBR361980A6TTGRCS
2022-06-15
Class II — The warning label was printed with the incorrect weight capacity. The correct weight limit is 400 lbs., but the label states 500 lbs.
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FDA Device Recall: OAKWORKS Inc.Lithotripsy/Urology Table: CFLU401, Catalog Number: 75216-T01 - Pro
2019-05-29
Class II — Table assembly error with incorrect actuators for the lateral and longitudinal table movements
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FDA Device Recall: Foot Controls impacted for the following devices: OAKWORKS¿ Medical CFPM 300
2018-03-07
Class II — 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 o...
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