Medical DeviceJan 24, 2024
Oakworks Ultrasound EA (Ergonomic Advantage) table versions recall — FDA Z-0729-2024
Backrest platform stress fracture - the table is not operational in an inclined position
Class IIFDA: OngoingOakworks Inc.
Recall history in this database
Classification mix: Class II: 6.
Medical DeviceJan 24, 2024
Oakworks Ultrasound EA (Ergonomic Advantage) table versions recall — FDA Z-0728-2024
Backrest platform stress fracture - the table is not operational in an inclined position
Class IIFDA: OngoingOakworks Inc.
Medical DeviceJan 24, 2024
Oakworks Ultrasound EA (Ergonomic Advantage) table version recall — FDA Z-0730-2024
Backrest platform stress fracture - the table is not operational in an inclined position
Class IIFDA: OngoingOakworks Inc.
Medical DeviceJan 24, 2024
Oakworks Ultrasound EA (Ergonomic Advantage) table versions recall — FDA Z-0727-2024
Backrest platform stress fracture - the table is not operational in an inclined position
Class IIFDA: OngoingOakworks Inc.
Medical DeviceJun 15, 2022
Oakworks PX200 Emergency Relief Bed recall — FDA Z-1238-2022
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.
Class IIFDA: TerminatedOakworks Inc.
Medical DeviceJun 15, 2022
Oakworks Bed (Emergency Field Bed) recall — FDA Z-1239-2022
The warning label was printed with the incorrect weight capacity. The correct weight limit is 400 lbs., but the label states 500 lbs.
Class IIFDA: TerminatedOakworks Inc.
Understanding this recall history
This page summarizes recall records in which the official source identifies Oakworks Inc. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.