Recall StatusTerminated
Date Initiated2020-08-24
Date Terminated2023-07-31
Product Quantity15 units
Reason for Recall
Steerable diagnostic catheter packages labeled Model IBI-81104, batch 7397352 incorrectly contained Model IBI-87002, batch 7397307. Packages labeled Model IBI-87002, batch 7397307 incorrectly contained Model IBI-81104, batch 7397352.If physicians fail to observe the catheter difference, the intracardiac electrograms will not be representative of the desired signals, could result in procedure delay
Firm Action
On 08/24/2020, Abbott Urgent Medical Device Recall Notices started being distributed to consignees in person or via mail.
Customers were advised to do the following:
1) Any remaining inventory from this affected lot should not be used.
2) Complete and return the Acknowledgment Form.
3) Return any remaining unused affected devices.
Please pass this notice to all those who need to be aware of it within your organization and maintain a record of this notice along with a copy of the completed Acknowledgement Form to ensure effectiveness of this communication. Should you have questions about this issue or for order replenishment, please contact your local firm Representative or Support at 1-855-478-5833 (Option 1) (U.S.), 7:00 a.m. - 7:00 p.m. Central Time, Monday through Friday.
Root Cause
Labeling mix-ups
Distribution Pattern
Worldwide distribution - U.S. Nationwide distribution including the states of MO, IN, WI, TX, AZ, MI, VA, KY and the country of Japan.
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.