FDA Device recall Z-0729-2024
Ultrasound EA (Ergonomic Advantage) table versions
- FDA Device
- Class II
- ongoing
- Published 2024-01-24
On 2024-01-24 the FDA classified a Class II recall of Ultrasound EA (Ergonomic Advantage) table versions by Oakworks, citing backrest platform stress fracture - the table is not operational in an inclined position.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0729-2024 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2023-12-05 |
| Published | 2024-01-24 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Oakworks |
| Distribution | US |
Product
Ultrasound EA (Ergonomic Advantage) table versions; G3 Multi-Specialty Echocardiography and Multi-Specialty with Electric Access Back Supports [left & right}
Reason
Backrest platform stress fracture - the table is not operational in an inclined position
Identifiers
| code_info | (UDI): 00817463025422 S/N: USM839457 USM839458 USM839459 USM839460 USM839461 USM818212 USM833897 USW813999 USM839614 U…(UDI): 00817463025422 S/N: USM839457 USM839458 USM839459 USM839460 USM839461 USM818212 USM833897 USW813999 USM839614 USM839615 USM814871 USM833507 USM831797 USM823858 USM822620 USM824500 USM834529 USM788091 USM815794 USM832170 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0729-2024%22
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