FDA Device recall Z-0068-2026
AW Server 2.0, AW Server 3.0, AW Server 3.1, AW Server 3.2
- FDA Device
- Class II
- ongoing
- Published 2025-10-15
On 2025-10-15 the FDA classified a Class II recall of AW Server 2.0, AW Server 3.0, AW Server 3.1, AW Server 3.2 by Ge Medical Systems Scs, citing firm has identified a security vulnerability in AW Server products. If exploited, a malicious actor could compromise the confidentiality, integrity, and availability of patient da….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0068-2026 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2025-09-05 |
| Published | 2025-10-15 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Ge Medical Systems Scs |
| Distribution | US |
Product
AW Server 2.0, AW Server 3.0, AW Server 3.1, AW Server 3.2
Reason
Firm has identified a security vulnerability in AW Server products. If exploited, a malicious actor could compromise the confidentiality, integrity, and availability of patient data.
Identifiers
| code_info | UDI-DI 00840682102384 System IDs 907729AWS1 720238AW1 907ULMCCT 205934AWSRV 205975AWSRV 205971AWS 205510VAW 205815AWS2…UDI-DI 00840682102384 System IDs 907729AWS1 720238AW1 907ULMCCT 205934AWSRV 205975AWSRV 205971AWS 205510VAW 205815AWS2 UABMAWS1 749153GE3 UABMRPET 256593AW1 256265AWS4 256265AWS3 205481AWS1 251343AWS 251665MCIAWS 251316VAWS 251435AW5 251435AWSMARTSUB1 303584HP To be provided 251435AWSSMARTSUB1 256386AW1 205RCAWS 870423AWSMARTSUB1 870642AWS 718329SMART11 479314AWS1 479314AWS2 870207AW1 501686AWS31 501978AW1 501686AWSMARTSUB2 501552AW2 501202AWS1 501686AWSMARTSUB1 479338AWS 928773AWS 928214AWS 480256AWS 928757AWEN To be provided pacsaws01 To be provided 602344AWS 602651AWS 480342AWS 602277REVAW 480342AWSMARTSUB2 480342AWSMART1 480342AWSMART2 602344AWS1 602344SMARTAW 480342AWS2 602BUMC870 480342AWSMARTSUB3 928445AW1 06A6A668-AW-AWS_PRIMARY 844823AW1 844823AW 928283AWSMARTSUB1 520STJAWS 818RIAWSVR 661CHAWS 661KMCAWS 13123 13767 650696AWS To be provided 530UCVETAWSERV To be provided 760633HDCT To be provided 714FVAWSERVER 714FVDISC 510792AWH 559326AWS1 714447AWS AVHHFCTAW1 858657AWSMARTSUB |
|---|
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-0068-2026%22
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