GE Inspection Technologies Blade|line Industrial Cabinet X-ray system — Class II medical device recall Z-2777-2017
Terminated recall by GE Inspection Technologies, LP, reported 2017-08-09, distributed in AL, MI, OH, PA, SC. GE Inspection Technologies, LP determined that the Blade|line cabinet x-ray system fails to comply with the ca
| Recall number | Z-2777-2017 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | FDA mandated |
| Recalling firm | GE Inspection Technologies, LP, Lewistown, PA, United States |
| Recall initiated | 2017-06-28 |
| Classified | 2017-08-01 |
| Reported by FDA | 2017-08-09 |
| Terminated | 2020-02-06 |
| Distributed | AL, MI, OH, PA, SC |
| Countries outside the US | DE, SG |
| Quantity | 13 units |
| Serial numbers | 158017R1, 201312TM, 201317TM, 201323TM, 201329TM, 201331TM, 201401TM, 201404TM, 201413TM, 201414TM, 201415TM, 201424TM, 201425 |
Product
GE Inspection Technologies Blade|line Industrial Cabinet X-ray system
Reason for recall
GE Inspection Technologies, LP determined that the Blade|line cabinet x-ray system fails to comply with the cabinet x-ray performance standards emission limit of 0.5 milliRoentgen in one hour (21 CFR ¿ 1020.40(c)(1)(i)) underneath the bottom center of the system. The crawl space affected by the excess emission is approximately 22 inches high, normally covered by decorative panels, and is not intended to be accessed.
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-2777-2017. 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.