FDA Device recall Z-0730-2024
Ultrasound EA (Ergonomic Advantage) table version
- 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 version 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-0730-2024 |
| 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 version; V2 (Vascular 2 Section) Echocardiography -An Ultrasound examination table
Reason
Backrest platform stress fracture - the table is not operational in an inclined position
Identifiers
| code_info | (UDI): 00817463025521 S/N: VCF805597 VCF814488 VCF814750 VCF817222 VCF817223 VCF817720 VCF817721 VCF823450 VCF825629 VC…(UDI): 00817463025521 S/N: VCF805597 VCF814488 VCF814750 VCF817222 VCF817223 VCF817720 VCF817721 VCF823450 VCF825629 VCF825630 VCF833350 VCF813968 VCF817520 VCF826533 VCF822117 VCF824501 VCF824502 VCF824503 VCF824504 VCF815120 VCF814849 VCF835728 |
|---|
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-0730-2024%22
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