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Manufacturers
Guidant Corp-Cpi Division
Manufacturer Address
Guidant Corp-Cpi Division, 4100 N Hamline Ave, St Paul MN 55112-5798
Source
USFDA
32 Events
Recall of Device Recall Guidant
Recall of Device Recall Guidant
Recall of Device Recall Guidant
Recall of Device Recall Guidant
Recall of Device Recall Guidant
Recall of Device Recall Guidant
Recall of Device Recall Guidant
Recall of Device Recall Guidant
Recall of Device Recall Guidant
Recall of Device Recall Guidant
Recall of Device Recall Guidant
Recall of Device Recall Guidant
Recall of Device Recall Guidant
Recall of Device Recall Guidant
Recall of Device Recall Guidant
Recall of Device Recall Guidant
Recall of Device Recall Guidant
Recall of Device Recall Guidant
Recall of Device Recall Guidant
Recall of Device Recall Guidant
Recall of Device Recall Guidant
Recall of Device Recall Guidant
Recall of Device Recall Guidant
Recall of Device Recall Guidant
Recall of Device Recall Guidant
Recall of Device Recall Guidant
Recall of Device Recall Guidant
Recall of Device Recall Guidant
Recall of Device Recall Guidant
Recall of Device Recall Guidant
Recall of Device Recall Guidant
Recall of Device Recall Guidant
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10 devices in the database
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
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
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
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
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
5 more
One manufacturer with a similar name
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Guidant Corp-Cpi Division
Manufacturer Address
Guidant Corp-Cpi Division, 4100 Hamline Ave N, Saint Paul MN 55112-5700
Source
USFDA
Language
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