Z-0990-2022 Class II Ongoing
FDA device recall Z-0990-2022 was initiated by St. Jude Medical, Cardiac Rhythm Management Division on March 10, 2022 and is designated Class II. Reason for recall: Bluetooth malfunction impacting Gallant devices post-implant. The failure causes the device to enter an inductive-only telemetry mode with a loss of Bluetooth communication. The Bluetooth malfunction… The recall status is ongoing. Affected quantity: 1.
Recall Details
- Product Type
- Devices
- Report Date
- April 27, 2022
- Initiation Date
- March 10, 2022
- Termination Date
- N/A
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 1
Product Description
Gallant HF Implantable Cardioverter Defibrillator REF# CDHFA500Q
Reason for Recall
Bluetooth malfunction impacting Gallant devices post-implant. The failure causes the device to enter an inductive-only telemetry mode with a loss of Bluetooth communication. The Bluetooth malfunction results in the inability to remotely monitor these devices and resulted in reduced battery longevity.
Distribution Pattern
Worldwide distribution - US Nationwide distribution in the states of FL, KY and the country of France, Czech Republic.
Code Information
REF# CDHFA500Q SN #111004346, Exp Date : 30-Jun-2022 Material # 100173746 UDI: 05415067032010