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Reviewed V1 category
Implantable cardiac devices that help manage slow or irregular heart rhythms.
FDA product codes and descriptions are normalized into this consumer-facing category. Raw regulator terminology remains source evidence rather than separate public category pages.
6 tracked devices · 1 recall record
Abbott · Pacemakers
No recall records foundLast checked Aug 17, 2026
BIOTRONIK SE & Co. KG · Pacemakers
No recall records foundLast checked Aug 17, 2026
Boston Scientific Corporation · Pacemakers
No recall records foundLast checked Aug 17, 2026
Medtronic, Inc. · Pacemakers
No recall records foundLast checked Aug 17, 2026
Medtronic, Inc. · Pacemakers
No recall records foundLast checked Aug 17, 2026
Software malfunction may occur during pacing capture threshold test of pacemaker resulting in programmer not successfully communicating the command to terminate the test.
Manufacturers are listed because their devices appear in monitored sources. Listing does not imply endorsement or partnership.
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