GE Healthcare — Class II medical device recall Z-1376-2015
Terminated recall by GE Healthcare, reported 2015-04-08, distributed in NC, OK. Specific Aespire 7900 Anesthesia Machines have an increased likelihood of failure of the CPU circuit board. Th
| Recall number | Z-1376-2015 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | GE Healthcare, Waukesha, WI, United States |
| Recall initiated | 2015-02-27 |
| Classified | 2015-04-02 |
| Reported by FDA | 2015-04-08 |
| Terminated | 2015-04-16 |
| Distributed | NC, OK |
| Countries outside the US | CN, IN, JP, MX, VE |
| Serial numbers | ANCU00101, ANCU00102, ANCU00103, ANCU00105, ANCU00108, ANCU00112, ANCU00113, ANCU00114, ANCU00115, ANCU00116, ANCU00117, ANCU00118, ANCU00119, ANCU00120, ANCU00121, ANCU00123, ANCU00124, ANCU00125, ANCU00126, ANCU00129, ANCU00130, ANCU00134, ANCU00135, ANCU00136, ANCU00137 and 21 more |
| Model numbers | 1009-9012-000 |
Product
GE Healthcare, Aespire 7900, Aespire View Anesthesia Machines. Model numbers 1009-9012-000. Intended to provide general inhalation anesthesia and ventilatory support to a wide range of patients
Reason for recall
Specific Aespire 7900 Anesthesia Machines have an increased likelihood of failure of the CPU circuit board. This could result in a blank display or loss of mechanical ventilation.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1376-2015. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.