Overview of recall records associated with St. Jude Medical, Atrial Fibrillation Division, Inc., including dates, categories and classifications where available.
Classification mix: Class II: 1.
When the catheters are used with the EnSiteX EP System, the system does not correctly recognize the catheter as the appropriate product model and instead reads and displays it as a…
This page summarizes recall records in which the official source identifies St. Jude Medical, Atrial Fibrillation Division, Inc. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.
