GE Healthcare — Class II medical device recall Z-1706-2016
Terminated recall by GE Medical Systems, LLC, reported 2016-06-01, distributed nationwide. Potential non-recoverable loss of image acquisition. The affected Discovery systems may experience multiple X-
| Recall number | Z-1706-2016 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | GE Medical Systems, LLC, Waukesha, WI, United States |
| Recall initiated | 2016-04-15 |
| Classified | 2016-05-23 |
| Reported by FDA | 2016-06-01 |
| Terminated | 2016-11-22 |
| Distributed | Nationwide (US) |
| Countries outside the US | AE, BE, CA, CN, DE, DZ, FR, GB, HU, IE, IT, JP, MX, NL, PE, SA, SG |
| Quantity | 54 |
| UPC / GTIN / UDI-DI | 00082416040061 |
Product
GE Healthcare, Discovery IGS 730. Indicated for use in generating fluoroscopic and rotational images of human anatomy.
Reason for recall
Potential non-recoverable loss of image acquisition. The affected Discovery systems may experience multiple X-Ray abort errors before or during a real-time fluoroscopic Interventional procedure.
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-1706-2016. 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.