FDA Device recall Z-0991-2024

Flow-e Anesthesia System, model 6887900

FDA Device
Class II
ongoing
Published 2024-02-14

On 2024-02-14 the FDA classified a Class II recall of Flow-e Anesthesia System, model 6887900 by Getinge Usa Sales, citing potential cybersecurity vulnerability that could lead to a Denial of Service (DoS) attack, tampering, or remote code execution via remote login to the Flow Anesthesia System, any….

Read the official FDA Device notice

Agency	FDA Device
Recall number	Z-0991-2024
Classification	Class II
Status	ongoing
Initiated	2023-12-11
Published	2024-02-14
Last updated	2026-09-13 11:57 UTC
Company	Getinge Usa Sales
Distribution	US

Product

Flow-e Anesthesia System, model 6887900

Reason

Potential cybersecurity vulnerability that could lead to a Denial of Service (DoS) attack, tampering, or remote code execution via remote login to the Flow Anesthesia System, any of which could lead to a hazardous situation.

Identifiers

code_info	UDI-DI: 07325710010457, serial numbers (US): 50012, 50030, 50031, 50033, 50034, 50035, 50036, 50037, 50038, 50039, 5004… UDI-DI: 07325710010457, serial numbers (US): 50012, 50030, 50031, 50033, 50034, 50035, 50036, 50037, 50038, 50039, 50040, 50041, 50042, 50043, 50046, 50047, 50048, 50051, 50052, 50053, 50054, 50055, 50056, 50057, 50058, 50059, 50060, 50069, 50070, 50071, 50072, 50073, 50074, 50084, 50085, 50086, 50087, 50088, 50089, 50090, 50091, 50092, 50093, 50094, 50096, 50097, 50108, 50109, 50110, 50111, 50132, 50154, 50155, 50193, 50194, 50195, 50196, 50197, 50199, 50211, 50212, 50213, 50214, 50215, 50216, 50217, 50218, 50219, 50220, 50221, 50223, 50224, 50225, 50244, 50245, 50246, 50247, 50248, 50249, 50250, 50251, 50252, 50253, 50254, 50276, 50277.

code_info

UDI-DI: 07325710010457, serial numbers (US): 50012, 50030, 50031, 50033, 50034, 50035, 50036, 50037, 50038, 50039, 5004…

UDI-DI: 07325710010457, serial numbers (US): 50012, 50030, 50031, 50033, 50034, 50035, 50036, 50037, 50038, 50039, 50040, 50041, 50042, 50043, 50046, 50047, 50048, 50051, 50052, 50053, 50054, 50055, 50056, 50057, 50058, 50059, 50060, 50069, 50070, 50071, 50072, 50073, 50074, 50084, 50085, 50086, 50087, 50088, 50089, 50090, 50091, 50092, 50093, 50094, 50096, 50097, 50108, 50109, 50110, 50111, 50132, 50154, 50155, 50193, 50194, 50195, 50196, 50197, 50199, 50211, 50212, 50213, 50214, 50215, 50216, 50217, 50218, 50219, 50220, 50221, 50223, 50224, 50225, 50244, 50245, 50246, 50247, 50248, 50249, 50250, 50251, 50252, 50253, 50254, 50276, 50277.

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-0991-2024%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.