FDA Device recall Z-0077-2025

Aespire View

FDA Device
Class I
ongoing
Published 2024-10-30

On 2024-10-30 the FDA classified a Class I recall of Aespire View by Datex Ohmeda, citing potential issue that may arise if the limb of a patient breathing circuit is mistakenly connected to the Auxiliary Common Gas Outlet (ACGO) port.

Read the official FDA Device notice

Agency	FDA Device
Recall number	Z-0077-2025
Classification	Class I
Status	ongoing
Initiated	2024-07-12
Published	2024-10-30
Last updated	2026-09-13 11:57 UTC
Company	Datex Ohmeda
Distribution	US

Product

Aespire View. This anesthesia gas machine is intended to provide general inhalation anesthesia and ventilatory support to patients and are to be used only by medical professionals trained and qualified in the administration of general anesthesia.

Reason

Potential issue that may arise if the limb of a patient breathing circuit is mistakenly connected to the Auxiliary Common Gas Outlet (ACGO) port.

Identifiers

code_info	GTIN: 00840682102285. Model Numbers: 1009-9212-000-117639, 1009-9212-000-136105, 1009-9212-000-518222, 1009-9212-000-52… GTIN: 00840682102285. Model Numbers: 1009-9212-000-117639, 1009-9212-000-136105, 1009-9212-000-518222, 1009-9212-000-521025, 1009-9212-000-552778, 1009-9212-000-090755, 1009-9212-000-059245, 1009-9212-000-110073, 1009-9212-000-203581, 1009-9212-000-423283, 1009-9212-000-419502, 1009-9212-000-427555, 1009-9212-000-460867, 1009-9212-000-478499, 1009-9212-000-109510, 1009-9212-000-521303, 1009-9212-000-097620, 1009-9212-000-102602, 1009-9212-000-520908, 1009-9212-000-098765, 1009-9212-000-076846, 1009-9212-000-070149, 1009-9212-000-189720, 1009-9212-000-140832, 1009-9212-000-036279, 1009-9212-000-484467, 1009-9212-000-520055, 1009-9212-000-516124, 1009-9212-000-182799, 1009-9212-000-161253, 1009-9212-000-121684, 1009-9212-000-117998, 1009-9212-000-499121, 1009-9212-000-405786, 1009-9212-000-425988, 1009-9212-000-309943, 1009-9212-000-045250, 1009-9212-000-121264, 1009-9212-000-478484, 1009-9212-000-184939, 1009-9212-000-513915, 1009-9212-000-049292, 1009-9212-000-467900, 1009-9212-000-521

code_info

GTIN: 00840682102285. Model Numbers: 1009-9212-000-117639, 1009-9212-000-136105, 1009-9212-000-518222, 1009-9212-000-52…

GTIN: 00840682102285. Model Numbers: 1009-9212-000-117639, 1009-9212-000-136105, 1009-9212-000-518222, 1009-9212-000-521025, 1009-9212-000-552778, 1009-9212-000-090755, 1009-9212-000-059245, 1009-9212-000-110073, 1009-9212-000-203581, 1009-9212-000-423283, 1009-9212-000-419502, 1009-9212-000-427555, 1009-9212-000-460867, 1009-9212-000-478499, 1009-9212-000-109510, 1009-9212-000-521303, 1009-9212-000-097620, 1009-9212-000-102602, 1009-9212-000-520908, 1009-9212-000-098765, 1009-9212-000-076846, 1009-9212-000-070149, 1009-9212-000-189720, 1009-9212-000-140832, 1009-9212-000-036279, 1009-9212-000-484467, 1009-9212-000-520055, 1009-9212-000-516124, 1009-9212-000-182799, 1009-9212-000-161253, 1009-9212-000-121684, 1009-9212-000-117998, 1009-9212-000-499121, 1009-9212-000-405786, 1009-9212-000-425988, 1009-9212-000-309943, 1009-9212-000-045250, 1009-9212-000-121264, 1009-9212-000-478484, 1009-9212-000-184939, 1009-9212-000-513915, 1009-9212-000-049292, 1009-9212-000-467900, 1009-9212-000-521

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-0077-2025%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.