Field replacement back up batteries distributed on or after April 1 — Class II medical device recall Z-1286-2022
Ongoing recall by GE Healthcare, LLC, reported 2022-07-06, distributed nationwide. Backup batteries can fail earlier than their estimated life.
| Recall number | Z-1286-2022 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | GE Healthcare, LLC, Waukesha, WI, United States |
| Recall initiated | 2022-04-25 |
| Classified | 2022-06-24 |
| Reported by FDA | 2022-07-06 |
| Distributed | Nationwide (US) |
| Countries outside the US | AE, AT, AU, BD, BE, BR, CH, CN, CR, CY, CZ, DE, DK, DZ, EG, ES, FR, GB, GR, HK, ID, IN, IQ, IT, JP, KE, KR, KW, LB, LT, LV, MA, MX, MY, NO, NP, NZ, OM, PA, PE, PH, PL, PT, RO, RU, SA, SE, SG, SK, TH, TR, TW, UA, VN, ZA |
| Quantity | 88,347 batteries |
Product
Field replacement back up batteries distributed on or after April 1, 2019 for Avance CS2, Avance CS2 Pro, Avance, Amingo, Aespire View anesthesia devices
Reason for recall
Backup batteries can fail earlier than their estimated life.
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-1286-2022. 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.