Devices

Device Recall Guidant

Model / Serial
Lots 4011451 and 4020551
Product Classification
Cardiovascular Devices
Device Class
2
Implanted device?
No
Distribution
Nationwide in the United States.
Product Description
Guidant Rapido 8 French Guiding Catheter, Inner Diameter .087'', 2.21 mm, Overall Length 54 cm, Coronary Sinus - Extended Hook Right Tip Shape, CS-EH R, REF 7592
Manufacturer
Guidant Corp-Cpi Division
2 Events
- Recall of Device Recall Guidant
- Recall of Device Recall Guidant

Manufacturer

Guidant Corp-Cpi Division

Manufacturer Address
Guidant Corp-Cpi Division, 4100 Hamline Ave N, Saint Paul MN 55112-5700
Source
USFDA

45 devices with a similar name

Learn more about the data here

Device Recall Guidant

Model / Serial
All Serial numbers
Product Classification
Cardiovascular Devices
Device Class
3
Implanted device?
Yes
Distribution
Nationwide in the United States and worldwide.
Product Description
Contak TR Multiprogrammable Pacemaker, DDDR Model 1241
Manufacturer
Guidant Corp-Cpi Division

Device Recall Guidant

Model / Serial
Serial number 105497
Product Classification
Cardiovascular Devices
Device Class
3
Implanted device?
Yes
Distribution
Nationwide in the United States and worldwide.
Product Description
Discovery II Multiprogrammable Pacemaker, Model 0481
Manufacturer
Guidant Corp-Cpi Division

Device Recall Guidant

Model / Serial
Serial numbers 110685, 110687, 110688, 110706, 110708, 110709, 110710, 110711, 110712, 110713 110714, and 110715
Product Classification
Cardiovascular Devices
Device Class
3
Implanted device?
Yes
Distribution
Nationwide in the United States and worldwide.
Product Description
Pulsar Max II Multiprogrammable Pacemaker, Model 1180
Manufacturer
Guidant Corp-Cpi Division

Device Recall Guidant

Model / Serial
Serial number 811798
Product Classification
Cardiovascular Devices
Device Class
3
Implanted device?
Yes
Distribution
Nationwide in the United States and worldwide.
Product Description
Pulsar Max II Multiprogrammable Pacemaker, Model 1181
Manufacturer
Guidant Corp-Cpi Division

Device Recall Guidant

Model / Serial
Serial numbers 206555, 206557, 206558, 206559, 206560, 206561, 206562, 206525, 206526, 206527, 206528, and 206529
Product Classification
Cardiovascular Devices
Device Class
3
Implanted device?
Yes
Distribution
Nationwide in the United States and worldwide.
Product Description
Discovery II Multiprogrammable Pacemaker, Model 0981
Manufacturer
Guidant Corp-Cpi Division

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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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The International Medical Devices Database is licensed under the Open Database License and its contents under Creative Commons Attribution-ShareAlike license. Always cite the International Consortium of Investigative Journalists when using this data. You can download a raw copy of the database here.

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