GE Inspection Technologies x|tome|x L240 an Cabinet X-ray system — Class II medical device recall Z-1211-2015
Terminated recall by GE Inspection Technologies, LP, reported 2015-04-01, distributed in OH, PA. It was discovered that the upper left corner-shaped lead shield in the window in one of the doors of the v|tom
| Recall number | Z-1211-2015 |
|---|---|
| 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 | 2015-01-13 |
| Classified | 2015-03-20 |
| Reported by FDA | 2015-04-01 |
| Terminated | 2015-08-17 |
| Distributed | OH, PA |
| Quantity | 2 |
Product
GE Inspection Technologies x|tome|x L240 an Cabinet X-ray system
Reason for recall
It was discovered that the upper left corner-shaped lead shield in the window in one of the doors of the v|tome|x L240 installed had lost adhesion and fall out of position, which could lead to gaps in shielding.
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-1211-2015. 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.