GE Inspection Technologies — Class II medical device recall Z-1231-2016
Terminated recall by GE Inspection Technologies, LP, reported 2016-04-13, distributed in AL, AZ, CA, CO, DC, FL, GA, ID…. GE Inspection Technologies, LP ("GE") has discovered that certain of its cabinet x-ray systems may not fully c
| Recall number | Z-1231-2016 |
|---|---|
| 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 | 2015-12-16 |
| Classified | 2016-04-01 |
| Reported by FDA | 2016-04-13 |
| Terminated | 2016-10-14 |
| Distributed | AL, AZ, CA, CO, DC, FL, GA, ID, IN, MA, MD, MI, MN, NC, NH, NJ, NY, OH, PA, SC, TN, TX, VA, WI |
| Quantity | 55 us |
Product
GE Inspection Technologies, LP, Cabinet X-ray system used for industrial quality control.
Reason for recall
GE Inspection Technologies, LP ("GE") has discovered that certain of its cabinet x-ray systems may not fully comply with the Food and Drug Administration's (FDA) Cabinet X¿ ray System performance standards, 21 C.F.R. ¿ 1020.40(c)(1)(i)
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-1231-2016. 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.