Product Safety Recalls

Product Recall Tracker

Abbott Recall 89872

Description: Abbott SE TactiCath Sensor Enabled Contact Force Ablation Catheter, Bi-D, Curve DD, Model A-TCSE-DD, Sterile.

Abbott Recall 89872 Information

StatusOngoing
Mandated?Voluntary: Firm initiated
Recall NumberZ-0957-2022
Event ID89872
Event DescriptionAbbott SE TactiCath Sensor Enabled Contact Force Ablation Catheter, Bi-D, Curve DD, Model A-TCSE-DD, Sterile.
Product TypeDevices
DistributionWorldwide distribution - US Nationwide - there was government distribution but no military. The countries of Austria, Belgium, Canada, Denmark, France, Germany, Greece, Israel, Italy, Japan, Netherlands, Norway, Palestine, Poland, Portugal, Russia, Slovakia, Spain, Sweden, Taiwan, and United Kingdom.
Quantity588 devices
Recall ReasonDevices were manufactured with a "First Use Date" preprogrammed in the EEPROM which disables the use of the single-use device.
Device Classification20220427
Device Code InfoLot numbers: 8181068, 8182131, 8198290, 8198350, 8200249, 8200300, 8201447, 8202313, 8203518, 8203835, 8203857, 8205760, and 8207547. UDI (01)05415067027634(17)230331(10)xxxxxxx (lot number).
Center Classification Date20220419
Recall Initiation Date20220324
Recalling FirmAbbott
Initial Notification Letter
Similar To

© 2022 Recall.Report / Contact / Privacy Policy

This site's data is aggregated programmatically and provided "as is" without any representations or warranties, express or implied.
Recall.report is not affiliated with the Consumer Product Safety Commision, FDA, or US government in any way.