FDA Device recall Z-0755-2017
GE Healthcare, Avance, Avance CS2, Amingo
- FDA Device
- Class II
- terminated
- Published 2016-12-21
On 2016-12-21 the FDA classified a Class II recall of GE Healthcare, Avance, Avance CS2, Amingo by Ge Healthcare, citing GE Healthcare has become aware of a potential safety issue where certain Avance CS2, Avance and Amingo anesthesia devices can transition to a System Malfunction state if the lower….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0755-2017 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2016-11-03 |
| Published | 2016-12-21 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Ge Healthcare |
| Distribution | US |
Product
GE Healthcare, Avance, Avance CS2, Amingo.
Reason
GE Healthcare has become aware of a potential safety issue where certain Avance CS2, Avance and Amingo anesthesia devices can transition to a System Malfunction state if the lower storage drawer containing the optional large tray insert accessory closed with an abnormally high amount of force.
Identifiers
| code_info | FMI 34079 Initial Consignee List Mfg. Lot or Serial # ANBM00775 ANBM00776 ANBM00779 ANBN00775 ANBR01060 APKS0103…FMI 34079 Initial Consignee List Mfg. Lot or Serial # ANBM00775 ANBM00776 ANBM00779 ANBN00775 ANBR01060 APKS01034 APKT00107 APKT02107 APKU00169 APKU00170 APKU00171 APKU01696 APKU01697 APKU01698 APKU01699 APKV00455 APKV00456 APKV00457 APKV00458 ANBH00259 ANBP00673 ANBP01851 ANBP02120 ANBP02121 APKS01352 APKS01353 APKS01354 APKS01355 APKS01356 APKT02322 APKT02323 APKT02324 APKT02325 APKT02326 APKV01600 APKV01601 APKV01602 APKV01554 APKV01555 APKV01556 APKV01557 APKV01558 APKV01559 APKV01560 APKV01561 APKV01562 APKV01198 APKV01199 APKV01200 APKV01201 ANBQ01418 ANBQ01419 ANBQ01420 ANBQ01421 ANBR01342 APKV00450 APKV00451 ANBM00230 ANBM00273 ANBM00497 ANBR00289 ANBR00290 ANBR00291 ANBR00292 ANBR00293 ANBR00294 ANBR00295 APKV01885 APKV01210 APKV01211 APKV00205 APKV00206 APKV00207 APKV00208 APKV00209 APKV00210 APKV00211 APKV00212 APKV00213 APKV00214 APKU00134 APKU00135 ANBQ01520 ANBQ01521 ANBQ01522 ANBQ01523 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0755-2017%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.