GE Cabinet X-ray systems — Class II medical device recall Z-0426-2015
Terminated recall by GE Inspection Technologies, LP, reported 2014-12-24, distributed in CA, IN, MI, NC, NH, OR, PA, SC…. GE discovered these cabinet x-ray systems' potential failure to comply with the Cabinet X-ray System performan
| Recall number | Z-0426-2015 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | GE Inspection Technologies, LP, Lewistown, PA, United States |
| Recall initiated | 2014-11-10 |
| Classified | 2014-12-17 |
| Reported by FDA | 2014-12-24 |
| Terminated | 2015-06-29 |
| Distributed | CA, IN, MI, NC, NH, OR, PA, SC, WA |
| Quantity | 11 |
| Serial numbers | A583730, A586430, A586460, A586590, A586780, VTX01F007-196312, VTX01LF007-208813, VTXO1FOO07-1946, VTXO1JOOO2-2245, VTXO1K0001-184711 |
Product
GE Cabinet X-ray systems
Reason for recall
GE discovered these cabinet x-ray systems' potential failure to comply with the Cabinet X-ray System performance standards.
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-0426-2015. 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.