Z-3011-2020 Class II Terminated
FDA device recall Z-3011-2020 was initiated by Irvine Biomedical Inc, a St. Jude Medical Co. on August 24, 2020 and is designated Class II. 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 containe… The recall status is terminated (terminated July 31, 2023). Affected quantity: 15 units.
Recall Details
- Product Type
- Devices
- Report Date
- September 30, 2020
- Initiation Date
- August 24, 2020
- Termination Date
- July 31, 2023
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 15 units
Product Description
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.
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
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.
Code Information
GTIN: 05414734302975, Lot: 7397352