FDA Device recall Z-0703-2019
Discover VH/Millennium VG Nuclear Medicine Imaging System
- FDA Device
- Class II
- completed
- Published 2019-01-16
On 2019-01-16 the FDA classified a Class II recall of Discover VH/Millennium VG Nuclear Medicine Imaging System by Ge Healthcare, citing 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….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0703-2019 |
| Classification | Class II |
| Status | completed |
| Initiated | 2017-10-30 |
| Published | 2019-01-16 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Ge Healthcare |
| Distribution | n/a |
Product
Discover VH/Millennium VG Nuclear Medicine Imaging System
Reason
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.
Identifiers
| code_info | Serial Numbers: 10191 10571 10269 1078 10340 10541 1081 10237 10326 1538 10171 1039 1080 10316 10177 10…Serial Numbers: 10191 10571 10269 1078 10340 10541 1081 10237 10326 1538 10171 1039 1080 10316 10177 10156 10197 10539 10395 1058 1372 10189 1107 1132 10438 10359 10406 10547 10375 10534 10182 3874990 10139 10555 1141 10354 10338 1056 10481 1035 10210 10572 10281 10190 10179 10193 1016 10300 10501 10284 10446 1119 10146 1100 10178 10041 00000011278NU9 3003 1126 10235 1013 10263 10526 10488 10507 10165 36478041 10239 10398 1025 10143 10390 10260 10435 10422 10445 10222 10357 10218 1046 10491 10353 10180 10530 5004 10256 10288 10333 10516 10556 10379 UNKASM00109201 10462 10557 10195 10581 10468 10560 10463 1890 10417 10334 DUMFMI40849011 10323 10425 10270 10426 1101 10453 10343 10348 10533 10412 10405 10494 DUMFMI40849005 10414 10561 10553 10461 10103 10352 10346 10529 1123 10213 10248 10371 10474 10023 1069 10385 1835 1118 1831 10362 10387 10393 1036 |
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Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: completed.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0703-2019%22
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