FDA Device recall Z-0917-2017
Shimadzu X-ray TV System, Catalog No. SONIALVISION G4
- FDA Device
- Class II
- terminated
- Published 2017-01-04
On 2017-01-04 the FDA classified a Class II recall of Shimadzu X-ray TV System, Catalog No. SONIALVISION G4 by Shimadzu Medical Systems, citing shimadzu Medical Systems is recalling Shimadzu X-ray TV System SONIALVISION due to possibility of oil leaking from the x-ray tube housing under certain conditions.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0917-2017 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2016-11-20 |
| Published | 2017-01-04 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Shimadzu Medical Systems |
| Distribution | AR, CA, CT, FL, GA, IA, IL, IN, MD, MT, NE, NV, NY, OH, OR, PA, SC, SD, TX, WA |
Product
Shimadzu X-ray TV System, Catalog No. SONIALVISION G4
Reason
Shimadzu Medical Systems is recalling Shimadzu X-ray TV System SONIALVISION due to possibility of oil leaking from the x-ray tube housing under certain conditions.
Identifiers
| code_info | Serial No. 41C351641002 41C351643001 41C351641003 41C351641001 41C351646001 41C351646002 41C351647001 41C35164A…Serial No. 41C351641002 41C351643001 41C351641003 41C351641001 41C351646001 41C351646002 41C351647001 41C35164A001 41C35164B001 41C35164C001 41C351651001 41C351651002 41C351653003 41C351653002 41C351653004 41C351653005 41C351654002 41C351655001 41C351655002 41C351655003 41C351656001 41C351659001 41C35165A001 41C35165A002 41C35165A003 41C35165B001 41C35165B002 41C351661001 41C351661002 41C351662001 41C351663001 41C351663002 41C351664001 41C351664002 41C351664004 41C351664005 41C351665001 41C351665003 41C351665002 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0917-2017%22
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