Biosense Webster, Inc.: Medical Device Recalls in 2017
Updated on March 25, 2026.
According to to data from the FDA, there were 8 medical device recalls made by Biosense Webster, Inc. in 2017. See the details of the recalls below.
You can see similar recalls for other firms.
Data Source: FDA.
- THERMOCOOL SMARTTOUCH Bi-Directional Navigation Catheter (D-132704-S, D-132705-S)
- THERMOCOOL SF NAV Catheters Model Numbers - BNI35FJCT, BNI35DFCT, D-131503-S, D-131504-S
- THERMOCOOL SMARTTOUCH SF Bi-Directional Product Codes D-1348-01-S, D-1348-04-S, D-1348-05-S
- PENTARAY NAV High-Density Mapping Catheter.
- PENTARAY NAV High-Density Mapping Catheter.
- SMARTABLATE RF System Generator
- THERMOCOOL SMARTTOUCH SF Uni-Directional Product Codes D-1347-01-S, D-1347-02-S, D-1347-03-S
- THERMOCOOL SMARTTOUCH Uni-Directional Navigation Catheter (D133602S)