Oakworks recalls Ultrasound EA and G3 Multi-Specialty Echocardiography tables due to backrest platform stress fractures when inclined. Affected units have specific serial numbers and UDI codes.
Backrest platform stress fracture - the table is not operational in an inclined position
Oakworks is recalling certain ultrasound tables because the backrest platform can fracture when tilted. This makes the table unsafe to use at an angle, potentially causing injury.
The backrest platform can develop stress fractures when the table is tilted. This causes the table to become non-operational in an inclined position, which could lead to injury if the table shifts unexpectedly.
Medical professionals using the Ultrasound EA or G3 Multi-Specialty Ech:chocardiography tables with specific serial numbers are most at risk. Patients using these tables during procedures may also be affected.
Check for serial numbers starting with USM839457 through USM839615 or USM814871, USM833507, USM831797, USM823858, USM822620, USM824500, USM834529, USM788091, USM815794, USM832170. The Unique Device Identifier (UDI) is 00817463025422.
Verify your table's serial number against the list of affected units provided in the recall notice.
The affected models are Ultrasound EA (Ergonomic Advantage) tables and G3 Multi-Specialty Echocardiography tables with Electric Access Back Supports.
Check for serial numbers starting with USM839457 through USM839615 or specific listed serial numbers like USM814871, USM833507, and USM831797. The Unique Device Identifier (UDI) is 00817463025422.
The recall notice does not specify a remedy, so contact Oakworks directly for further instructions.
We’ve drafted a message you can send Oakworks to request your refund or repair — edit it as you like.
Subject: Recall Z-0729-2024 — Oakworks Oakworks Hello, I own a Oakworks that is covered by recall Z-0729-2024 from Oakworks. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
