Discover VH/Millennium VG Nuclear Medicine Imaging System — Class II medical device recall Z-0703-2019
Completed recall by GE Healthcare, LLC, reported 2019-01-16. A potential hazardous situation may occur if the collimator locking handle is not properly placed in the lock
| Recall number | Z-0703-2019 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Completed |
| Voluntary or mandated | Voluntary |
| Recalling firm | GE Healthcare, LLC, Waukesha, WI, United States |
| Recall initiated | 2017-10-30 |
| Classified | 2019-01-09 |
| Reported by FDA | 2019-01-16 |
| Quantity | 339 units |
| Serial numbers | 00000011278NU9, 0000D4360X4372, 10023, 10028, 1003, 10040, 10041, 10057, 1006, 1010, 10103, 10121, 10124, 1013, 10133, 10139, 10143, 10146, 10156, 10158, 1016, 10164, 10165, 10167, 10169 and 311 more |
Product
Discover VH/Millennium VG Nuclear Medicine Imaging System
Reason for recall
A potential hazardous situation may occur if the collimator locking handle is not properly placed in the lock position and the warning circuit does not detect that the collimator is unlocked because of the patient proximity to the collimator during a clinical scan.
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-0703-2019. 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.