RecallRadar

FDA Device recall Z-1389-2022

GE Healthcare Aisys CS2 Anesthesia System, Part number 1011-9050-000

On 2022-07-27 the FDA classified a Class I recall of GE Healthcare Aisys CS2 Anesthesia System, Part number 1011-9050-000 by Ge Healthcare, citing there is a potential reversal of the O2 and air cylinder pressure transducer connections.

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-1389-2022
ClassificationClass I
Statusterminated
Initiated2022-06-01
Published2022-07-27
Last updated2026-09-13 11:56 UTC
CompanyGe Healthcare
DistributionUS

Product

GE Healthcare Aisys CS2 Anesthesia System, Part number 1011-9050-000; and Avance CS2 and Avance CS2 Pro Anesthesia System, Part number 1009-9050-000.

Reason

There is a potential reversal of the O2 and air cylinder pressure transducer connections.

Identifiers

code_info
Aisys CS2 - GTIN 00840682102292 Serial numbers starting with APWA: 00101 through 00176, 00185 through 00697, 00700 t…Aisys CS2 - GTIN 00840682102292 Serial numbers starting with APWA: 00101 through 00176, 00185 through 00697, 00700 through 00763, 00768 through 01013, 01016 through 01216, 01218 through 01223, 01225 through 01596, 01601 through 01683, 01685 through 01805, 01808 through 01960, 01964 through 01999, 02003 through 02021, 02026 through 02168, 02175, 02182 through 02308, 02311 through 02361, 02376 through 02405, 02424 through 02429, 02450 through 02456, 02519 through 02531, 02533 through 02539. Serial numbers starting with APWB: 00101 through 00151, 00154, 00155, 00162, 00163, 00169 through 00199, 00201 through 00336, 00338 through 00373, 00378 through 00644, 00647 through 00684, 00686 through 00689, 00691 through 00743, 00746 through 00750, 00754 through 00756, 00770 through 00818, 00823 through 00828, 00838 through 00842, 00905 through 00931, 00944 through 00952. Serial numbers starting with APWZ: 03034 through 03037, 03053 through 03056, 03060, 03062 through 03066, 03071 through 03

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1389-2022%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.