Oakworks Inc

Complete recall history across all FDA and CPSC categories — 9 total recalls

Oakworks Inc appears in recall records across 1 category. This page consolidates all FDA food, drug, and medical device enforcement actions, plus CPSC consumer product recalls associated with this company. Recall data is sourced from openFDA and CPSC public databases.

Device Recalls (9)

FDA medical device enforcement actions by Oakworks Inc

Date Product Reason Class
Dec 5, 2023 Ultrasound EA (Ergonomic Advantage) table versions; G2 (GENERAL 2) -An Ultras... Backrest platform stress fracture - the table is not operational in an inclin... Class II
Dec 5, 2023 Ultrasound EA (Ergonomic Advantage) table version; V2 (Vascular 2 Section) Ec... Backrest platform stress fracture - the table is not operational in an inclin... Class II
Dec 5, 2023 Ultrasound EA (Ergonomic Advantage) table versions; G3 (General 3 Section) Ec... Backrest platform stress fracture - the table is not operational in an inclin... Class II
Dec 5, 2023 Ultrasound EA (Ergonomic Advantage) table versions; G3 Multi-Specialty Echoca... Backrest platform stress fracture - the table is not operational in an inclin... Class II
Apr 21, 2022 Oakworks Bed (Emergency Field Bed); Model No. OBMPBR361980A6TTGRCS The warning label was printed with the incorrect weight capacity. The correct... Class II
Apr 21, 2022 PX200 Emergency Relief Bed; Model No. PXEXEB362280A6TTZZH4C19 Product label was printed without the UDI number and warning label was printe... Class II
Jun 29, 2021 Vascular Table without Fowler (USV1) and Ultrasound Vascular Table with Fowle... Weld failure- the bracket attaches the tabletop tilting actuator to the table... Class II
May 2, 2019 OAKWORKS Inc.Lithotripsy/Urology Table: CFLU401, Catalog Number: 75216-T01 - ... Table assembly error with incorrect actuators for the lateral and longitudina... Class II
Jul 31, 2017 Foot Controls impacted for the following devices: OAKWORKS¿ Medical CFPM 3... The foot control used on the OAKWORKS¿ Inc., CFPM300, CFPM301, CFPM400, CFPM4... Class II

Frequently Asked Questions

A high number of recalls does not necessarily indicate that a company is unsafe. Large manufacturers that produce thousands of products across multiple categories will statistically appear in recall databases more frequently. What matters more is the severity of each recall (Class I being the most serious), the speed of response, and whether the company proactively identified and addressed the issue. Companies with robust safety programs often catch problems earlier.

Food, drug, and medical device recall data comes from the FDA's openFDA enforcement database, which contains all FDA enforcement reports. Consumer product recall data comes from the U.S. Consumer Product Safety Commission (CPSC). Both sources are public government databases that are updated regularly. RecallCheck aggregates these sources to provide a unified view of a company's recall history.

The FDA classifies recalls into three categories. Class I is the most serious — there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. Class II means the product may cause temporary or medically reversible health problems, or the probability of serious consequences is remote. Class III is the least serious — the product is unlikely to cause adverse health consequences. CPSC product recalls do not use this classification system.

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