FDA Device recall Z-1585-2016
X-Ray Diagnostic Table, Model No. YSF-300 Use in combination with an X-ray high voltage generator, an X-ray tube unit, an Image intensifier…
- FDA Device
- Class II
- terminated
- Published 2016-05-04
On 2016-05-04 the FDA classified a Class II recall of X-Ray Diagnostic Table, Model No. YSF-300 Use in combination with an X-ray high voltage generator, an X-ray tube unit, an Image intensifier… by Shimadzu Medical Systems, citing report of unintentional movement of table to reverse tilting.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1585-2016 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2016-03-31 |
| Published | 2016-05-04 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Shimadzu Medical Systems |
| Distribution | US |
Product
X-Ray Diagnostic Table, Model No. YSF-300 Use in combination with an X-ray high voltage generator, an X-ray tube unit, an Image intensifier and X-ray television unit, this table is applied for the following X-ray examinations: -X-ray T.V. fluoroscopy -Spot-filming -Bucky radiography
Reason
Report of unintentional movement of table to reverse tilting.
Identifiers
| code_info | Serial No. 0162A80301 0162A80302 0162A80303 0162A80401 0162A80403 0162A81001 0162A81002 0162A81003 0162A81101…Serial No. 0162A80301 0162A80302 0162A80303 0162A80401 0162A80403 0162A81001 0162A81002 0162A81003 0162A81101 0162A81102 0162A81103 0162A81104 0162A81105 0162A81106 0162A81301 0162A81302 0162A81303 0162A81304 0162A81501 0162A81502 0162A81503 0162A81504 0162A81505 0162A81601 0162A81602 0162A81603 0162A81701 0162A81702 0162A81703 0162A81704 0162A81705 0162A81801 0162A81803 0162A82101 0162A82102 0162A82202 0162A82203 0162A82301 0162A82302 0162A82501 0162A82502 0162A82601 0162A82602 0162A82701 0162A82702 0162A82703 0162A82801 0162A82802 0162A82902 0162A83001 0162A83002 0162A83101 0162A83201 0162A83202 0162A83301 0162A83302 0162A83401 0162A83501 0162A83502 0162A83601 0162A83602 0162A83702 0162A83801 0162A83901 0162A83902 0162A84001 0162A84101 0162A84102 0162A84201 0162A84202 0162A84203 0162A84301 0162A84302 0162A84401 0162A84402 0162A84501 0162A84502 0162A84601 0162A84602 0162A84701 0162A84702 0162A84802 0162 |
|---|
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-1585-2016%22
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