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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
Serial numbers 547737, 547738, 547739, 547740, 547741, 547742, 547744, 547745, 547746, 547747, 547748, 547749, 547751, 547753, 547754, and 547964
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 1280
Device Recall Guidant
Model / Serial
Serial numbers 908813, 908814, 908817, 908819, 908820
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 1286
Device Recall Guidant
Model / Serial
Serial numbers 721824, 721825, 721826, 721827, 721828, 721829, 721830, 721831, 721832, 721833, 721834, 721835, 721836, 721837, 721838, 721839, 721840, 721841, 721843, 721908, 721909, 721910, 721911, 721912, 721913, 721914, 721915, 721916, 721917, 721918, 721919, 721920, 721921, 721922, 721923, 721924, 721926, 721927, 721928, 721929, 721930, 721931, 721932, 721933, 721934, 721935, 721936, 721937, 721938, and 721939
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 1284
Device Recall Guidant
Model / Serial
Serial numbers 639293, 639295, and 639296
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 1283
Device Recall Guidant
Model / Serial
Serial numbers 319492, 319493, 319494, 319495, 319496, 319497, 319498, 319499, 319500, 319501, 319502, 319503, 319505, 319506, and 319507
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 1184
5 more
One manufacturer with a similar name
Learn more about the data
here
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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