Recall Register

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Shimadzu Medical Systems Usa Com

FDA recalling firm · 5 enforcement events · 7 product records · 2017–2019 · CA

Shimadzu Medical Systems Usa Com has 5 FDA enforcement events on this register (7 product records) between 2017 and 2019: 5 device; the busiest year was 2019 with 3.

0% of its events are Class I; the most common class is Class II (5). 0 events are listed as ongoing; the recalling firm's address is in CA.

Recall classification reflects the relative degree of health hazard. Event counts depend on a firm's size and product range; they are not a comparison of one firm with another.

Enforcement events

InitiatedProduct (first record)TypeClassRecordsStatus
14 Jan 2019BRANSIST safire Product Usage: DIGITAL ANGIOGRAPHY SYSTEM This system is intended to be used for radiologic visualization of the heart, blood vessels or lymphatic system during or after injection of a contrast medium. It is to be used in the diagnosis of the circulatory vascular system while being combined with a…DeviceClass II1Terminated
14 Jan 2019SHIMADZU MobileDaRt Evolution (MX8 Version), Mobile X-Ray System Product Usage: This device is intended to be used to take a film, CR or general radiography of patients in the hospital who cannot move and/or of outpatients in emergency. Exposure can be captured on film, CR or Digital Radiography (DR).DeviceClass II1Terminated
14 Jan 2019TRINIAS for diagnostic imaging and interventional procedures in cardiac angiography, neurovascular angiography, abdominal angiography, peripheral angiography, rotational angiography, multi-purpose angiography and whole body radiographic/fluoroscopic procedures.DeviceClass II1Terminated
15 Jun 2018TRINIAS Digital Angiographic System intended to be used for cardiac angiography, neurovascular angiography, abdominal angiography, peripheral angiography, rotational angiography, multi-purpose angiography and whole body radiographic/fluoroscopic procedures.DeviceClass II1Terminated
23 May 2017SHIMADZU Ceiling Type X-ray Tube Support CH-200/CH-200M Catalog Number: CH-200/CH-200M Holds an x-ray tube unit and collimator combined with an z-ray high voltage generator, radiographic stand, and table. It is designed to perform radiography of patients either in a standing or supine positionDeviceClass II3Terminated

By type and class

Device5
Class II5

Class I: 0% of this firm's events; 18% of all events on the register.

Events by year

17
18
19
20
21
22
23
24
25
26
Enforcement events for Shimadzu Medical Systems Usa Com by year initiated.

Questions and answers

How many FDA recalls has Shimadzu Medical Systems Usa Com had?

5 enforcement events (7 product records) on this register, 2017–2019: 5 device.

Are any Shimadzu Medical Systems Usa Com recalls ongoing?

0 events are listed as ongoing in the current openFDA export.

What class are Shimadzu Medical Systems Usa Com recalls?

5 Class II. 0% are Class I against 18% of all events on the register. Class reflects the relative degree of health hazard of the product, not the firm.

Where does this data come from?

openFDA food, drug and device enforcement reports (CC0), export dated 28 Sep 2026.

Provenance

Source: openFDA enforcement reports (CC0), export dated 28 Sep 2026. Firm names are grouped exactly as FDA spells them; the same company can appear under several spellings. Only organisations are shown. See the methodology.