Data Foundry

Medical device recalls 2016

X-Ray Diagnostic Table — Class II medical device recall Z-1585-2016

Terminated recall by Shimadzu Medical Systems, reported 2016-05-04, distributed nationwide. Report of unintentional movement of table to reverse tilting.

Recall numberZ-1585-2016
Product typeMedical device
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmShimadzu Medical Systems, Torrance, CA, United States
Recall initiated2016-03-31
Classified2016-04-28
Reported by FDA2016-05-04
Terminated2017-01-02
DistributedNationwide (US)
Quantity185 units
Serial numbers0162A80301, 0162A80302, 0162A80303, 0162A80401, 0162A80403, 0162A81001, 0162A81002, 0162A81003, 0162A81101, 0162A81102, 0162A81103, 0162A81104, 0162A81105, 0162A81106, 0162A81301, 0162A81302, 0162A81303, 0162A81304, 0162A81501, 0162A81502, 0162A81503, 0162A81504, 0162A81505, 0162A81601, 0162A81602 and 160 more
Model numbersYSF-300

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 for recall

Report of unintentional movement of table to reverse tilting.

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-1585-2016. 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.