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Product Description
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Recall Class
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FDA Recall Posting Date
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Recalling Firm
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Z-0260-2013 - R-30H , Diagnostic X-Ray Beam-Limiting Device.
In combination with any of below X-ray tubes
0.6/1.2P364DK-85, 0.6/1.2P324DK-125,
0.6/1.2P324DK-85, 0.6/1.2P38DE-85
Device Model # R-30H.
...
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2
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11/08/2012
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FEI # 1000125362 Shimadzu Medical Systems
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Z-0261-2013 - R-20J , Diagnostic X-Ray Beam-Limiting Device.
In combination with any of below X-Ray tubes:
06/1.2P364DK-85, 0.6/1.2P324DK-125,
06/1.2P324DK-85, 0.6/1.2P38DE-85.
Product Usage:
The device i...
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2
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11/08/2012
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FEI # 1000125362 Shimadzu Medical Systems
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Z-0265-2013 - 0.4/0.7JG326D-265AX/AT
Product Usage:
The device is a mobile X-ray system in order to take general radiography of patients in the hospital who cannot move and/or of outpatients in emergency.
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2
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11/08/2012
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FEI # 1000125362 Shimadzu Medical Systems
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Z-0263-2013 - 0.7/1.3U163CS-36
In combination with below systems
MobileArt Evolution, MobileDaRt Evolution
Product Usage:
The device is a mobile X-ray system in order to take general radiography of patients i...
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2
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11/08/2012
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FEI # 1000125362 Shimadzu Medical Systems
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Z-0264-2013 - 0.7/1.2JG326D-265
Product Usage:
The device is a mobile X-ray system in order to take general radiography of patients in the hospital who cannot move and/or of outpatients in emergency.
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2
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11/08/2012
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FEI # 1000125362 Shimadzu Medical Systems
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Z-0262-2013 - 0.7U163CS-36
In combination with below systems
MUX-100H, MUX-100D, MobileArt Evolution
Brand Name: MUX-100H.
Classification Name: Mobile x-ray system.
Device Model#MUX-100H.
Product Usag...
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2
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11/08/2012
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FEI # 1000125362 Shimadzu Medical Systems
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