Devices

Device Recall

Model / Serial
Product Classification
General Hospital and Personal Use Devices
Device Class
2
Implanted device?
No
Distribution
Distribution was nationwide in the United States. There were no U.S. government accounts.
Manufacturer
3m Health Care
1 Event
- Recall of Device Recall

Manufacturer

3m Health Care

Manufacturer Address
3m Health Care, 3m Center, Saint Paul MN 55144-1001
Source
USFDA

22687 devices with a similar name

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Device Recall syngo US Workplace

Model / Serial
Material number: 10035829, serial numbers: 250576, 260044, 260049, 260016, 250533, 250548, 250544, 250545, 250591, 250595, 250617, 700464562, 700465913, 700465914, 250565, 250557, and 250556.
Product Classification
Radiology Devices
Device Class
2
Implanted device?
No
Distribution
Worldwide Distribution: South Korea, Malaysia, Lithuania and China, and 1 unit to New Jersey in the USA.
Product Description
syngo US Workplace Picture Archiving and Communication System, software version 2.0, Siemens Medical Solutions, Inc., Mountain View, CA 94043
Manufacturer
Siemens Medical Solutions USA, Inc.

Device Recall Dura Star

Model / Serial
Lot #: 13193169 13231743 13237267 13266367 13269602 13271042 13272422 13299493 13303055 and 13314184
Product Classification
Cardiovascular Devices
Device Class
2
Implanted device?
No
Distribution
Worldwide.
Product Description
CORDIS "Dura Star" 2.25 x 10 Dilatation Catheter, Catalog # 70110225, Distributed by Cordis Corporation, Miami Lakes, FL 33014
Manufacturer
Cordis Corporation

Device Recall Dura Star

Model / Serial
Lot #s: 13175336 13180557 13189422 13190774 13208064 13209913 13209921 13211074 13217606 13225515 13245564 13250081 13251126 13252416 13266368 13269603 13272936 13278669 13285514 13289737 13297291 13298192 13300591 13303777 13305476 13309104 and 13314185
Product Classification
Cardiovascular Devices
Device Class
2
Implanted device?
No
Distribution
Worldwide.
Product Description
CORDIS "Dura Star" 2.50 x 10 Dilatation Catheter, Catalog # 70110250, Distributed by Cordis Corporation, Miami Lakes, FL 33014
Manufacturer
Cordis Corporation

Device Recall Dura Star

Model / Serial
Lot #s: 13193167 13208065 13212428 13222114 13249530 13250702 13250954 13266369 13269604 13271043 13272423 13298187 13298780 13305478 and 13309106
Product Classification
Cardiovascular Devices
Device Class
2
Implanted device?
No
Distribution
Worldwide.
Product Description
CORDIS "Dura Star" 2.75 x 10 Dilatation Catheter, Catalog # :70110275, Distributed by Cordis Corporation, Miami Lakes, FL 33014
Manufacturer
Cordis Corporation

Device Recall Dura Star

Model / Serial
Lot #s: 13175335 13180558 13182673 13189425 13198875 13207206 13208066 13209922 13211075 13217618 13237269 13245566 13251127 13255234 13266370 13269605 13271045 13272424 13275164 13281459 13281460 13281461 13282478 13287294 13289742 13291882 13298188 13298781 13302297 13312712 13312716 and 13313278
Product Classification
Cardiovascular Devices
Device Class
2
Implanted device?
No
Distribution
Worldwide.
Product Description
CORDIS "Dura Star" 3.00 x 10 Dilatation Catheter, Catalog # 70110300, Distributed by Cordis Corporation, Miami Lakes, FL 33014
Manufacturer
Cordis Corporation

22682 more

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Disclaimer

Medical devices help to diagnose, prevent and treat many injuries and diseases. We are not suggesting or implying that any companies or other entities included in the International Medical Devices Database engaged in unlawful conduct or otherwise acted improperly. The same device may have different names in different countries. This database is not intended to provide medical advice and patients should check with their doctors to determine if it contains relevant information and if such information has medical implications for them.

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