FDA recall Z-1344-2022

Abbott · Class II · device

Product

Abbott TactiCath Sensor Enabled, Contact Force Ablation Catheter, 8F 115cm FJ, REF A-TCSE-FJ. For mapping of the heart chambers during ablation.

Reason for recall

When connected to the EnSite Precision Navigation System, an affected TactiCath Contact Force Ablation Catheter, Sensor Enabled may present the error message: "invalid catheter,, or "expired catheter."

Distribution

US Nationwide distribution.

Key facts

Status
Ongoing
Initiation date
2022-06-09
Report date
2022-07-13
Voluntary/Mandated
Voluntary: Firm initiated
Location
Plymouth, MN, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1344-2022