Irvine Biomedical Inc, a St. Jude Medical Co. Inquiry Steerable Diagnostic Catheter, REF: IBI-81104 - Product Usage: INDICATIONS FOR USE The Inquiry fixed curve and steerable electrophysiology catheters are used for electrogram recording and cardiac stimulation during diagnostic electrophysiology studies. The catheters are commonly placed at the high right atrium, right ventricular apex, and HIS bundle. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Inquiry Steerable Diagnostic Catheter, REF: IBI-81104 - Product Usage: INDICATIONS FOR USE The Inquiry fixed curve and steerable electrophysiology catheters are used for electrogram recording and cardiac stimulation during diagnostic electrophysiology studies. The catheters are commonly placed at the high right atrium, right ventricular apex, and HIS bundle.
Brand
Irvine Biomedical Inc, a St. Jude Medical Co.
Lot Codes / Batch Numbers
GTIN: 05414734302975, Lot: 7397352
Products Sold
GTIN: 05414734302975, Lot: 7397352
Irvine Biomedical Inc, a St. Jude Medical Co. is recalling Inquiry Steerable Diagnostic Catheter, REF: IBI-81104 - Product Usage: INDICATIONS FOR USE The Inqui due to Steerable diagnostic catheter packages labeled Model IBI-81104, batch 7397352 incorrectly contained Model IBI-87002, batch 7397307. Packages labeled M. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
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
Recommended Action
Per FDA guidance
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.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026