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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 77351

3 recalled-product records grouped only because every row carries this exact official event ID.

Open FDA event record

Event summary

Timeline bucket
May 23, 2017
Product types
Device
Classifications
Class II
Statuses
Terminated
Recalling firm wording
Shimadzu Medical Systems Usa Com

Dossier provenance

Source snapshots represented here

  • openFDA Device Enforcement Report-date coverage June 20, 2012–July 08, 2026 Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.
  • openFDA Device Recall event_date_initiated coverage June 01, 1997–June 30, 2026

Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.

How coverage and grouping work

Complete imported group

Every recalled product in this event

3 official enforcement rows

Product dates, classifications, firms, and source wording remain attached to their individual rows. Opening this dossier never hides products that did not match a prior timeline filter.

device · product 1 of 3

SHIMADZU 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 position

Z-2653-2017
Recall number
Z-2653-2017
Initiated
May 23, 2017
Classification
Class II
Status
Terminated
Quantity
1673 units total

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Cracks may occur over time on the tube holding shaft near the base of the tube mounting flange.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Device Design

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Cracks may occur over time on the tube holding shaft near the base of the tube mounting flange.

Code information

Serial No. 0162M4501 thru 0562M45103, 3ZC5C2A0C002 thru 3ZC5C1734001, D362M42902 thru 0562M41101, 41E733E69003, MP95A8F5A001 thru MP95A9F6B001

Distribution pattern

Worldwide Distribution - Nationwide distribution to AK, AR, AZ, CA, CT, FL, IL, IN, KS, LA, MI, MO, NE, NJ, NM, NV, NY,OH, OK, PA, RI, SC, TN, TX, WA, WI, and Hawaii Foreign: Canada and Japan

device · product 2 of 3

SHIMADZU RADspeed Pro Catalog Number: RADspeed Pro; Stationary x-ray system

Z-2654-2017
Recall number
Z-2654-2017
Initiated
May 23, 2017
Classification
Class II
Status
Terminated
Quantity
1673 units total

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Cracks may occur over time on the tube holding shaft near the base of the tube mounting flange.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Device Design

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Cracks may occur over time on the tube holding shaft near the base of the tube mounting flange.

Code information

Serial No. 0162M4501 thru 0562M45103, 3ZC5C2A0C002 thru 3ZC5C1734001, D362M42902 thru 0562M41101, 41E733E69003, MP95A8F5A001 thru MP95A9F6B001

Distribution pattern

Worldwide Distribution - Nationwide distribution to AK, AR, AZ, CA, CT, FL, IL, IN, KS, LA, MI, MO, NE, NJ, NM, NV, NY,OH, OK, PA, RI, SC, TN, TX, WA, WI, and Hawaii Foreign: Canada and Japan

device · product 3 of 3

SHIMADZU FDR Visionary Catalog Number: FDR Visionary Suite Stationary x-ray system for taking general radiographic and tomographic images of the whole body. The device is intended to be used in hospitals, clinics, imaging centers, and/or other healthcare facilities by qualified/trained professionals

Z-2655-2017
Recall number
Z-2655-2017
Initiated
May 23, 2017
Classification
Class II
Status
Terminated
Quantity
1673 units total

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Cracks may occur over time on the tube holding shaft near the base of the tube mounting flange.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Device Design

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Cracks may occur over time on the tube holding shaft near the base of the tube mounting flange.

Code information

Serial No. 0162M4501 thru 0562M45103, 3ZC5C2A0C002 thru 3ZC5C1734001, D362M42902 thru 0562M41101, 41E733E69003, MP95A8F5A001 thru MP95A9F6B001

Distribution pattern

Worldwide Distribution - Nationwide distribution to AK, AR, AZ, CA, CT, FL, IL, IN, KS, LA, MI, MO, NE, NJ, NM, NV, NY,OH, OK, PA, RI, SC, TN, TX, WA, WI, and Hawaii Foreign: Canada and Japan