Canister: CO2 canister with GE part numbers 1407-3200-000 — Class II medical device recall Z-1443-2013
Terminated recall by GE Healthcare, LLC, reported 2013-06-12, distributed nationwide. GE Healthcare has recently become aware of a potential safety issue involving the reusable CO2 absorbent canis
| Recall number | Z-1443-2013 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | GE Healthcare, LLC, Waukesha, WI, United States |
| Recall initiated | 2013-05-14 |
| Classified | 2013-06-02 |
| Reported by FDA | 2013-06-12 |
| Terminated | 2014-03-12 |
| Distributed | Nationwide (US) |
| Countries outside the US | AE, AU, BD, BH, BO, BR, CA, CL, CN, CO, CZ, DE, EG, FI, FR, GB, HK, HU, ID, IL, IN, IQ, IT, JP, KR, LB, MX, MY, NZ, OM, PE, PH, PY, RS, SA, SG, SK, SV, TH, TR, VN, ZA |
| Quantity | 800 |
| Reason classes | packaging |
| Model numbers | 1407-3200-000, 1407-7004-000, M1084850 |
Product
Canister: CO2 canister with GE part numbers 1407-3200-000, 1407-7004-000, or M1084850. Intended to provide general inhalation anesthesia and ventilatory support.
Reason for recall
GE Healthcare has recently become aware of a potential safety issue involving the reusable CO2 absorbent canister accessory used with Aespire, Aespire View, Avance, Avance CS2, Aisys, ADU, 9100, M900, M904, 9300 systems. Reusable CO2 absorbent canisters accessories may not seal properly.
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-1443-2013. 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.