St Jude Medical is a leading manufacturer of medical devices and implants, specializing in cardiac care solutions. Their products include pacemakers, defibrillators, and other cardiac devices.
The firm is releasing new firmware for high voltage implantable cardiac devices (ICD) and cardiac resynchronization therapy defibrillators (CRT-D) intended to strengthen security by providing an additional layer of protection against unauthorized device access. For older generation devices not capable of accepting the firmware, the firm is advising customers of the option to permanently disable the RF communication capability in these devices.
St Jude Medical is a leading manufacturer of medical devices and implants, specializing in cardiac care solutions. Their products include pacemakers, defibrillators, and other cardiac devices.
The company is a legitimate medical device manufacturer with a strong reputation in cardiac care. Their products are designed to be safe and effective for patients with cardiac conditions.
Patients with cardiac conditions
Check for the product name, model number, and any specific warnings or instructions provided with the device.
Identify the specific product model and its intended use.
Ensure the device is approved by relevant regulatory bodies (e.g., FDA).
Consult with a healthcare professional for any concerns about the device.
Yes, St Jude Medical is a leading manufacturer of medical devices and implants, specializing in cardiac care solutions.
St Jude Medical produces pacemakers, defibrillators, and other cardiac devices.
Ensure the device is approved by relevant regulatory bodies (e.g., FDA) and consult with a healthcare professional for any concerns.
We’ve drafted a message you can send St Jude Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-2322-2018 — St Jude Medical St Jude Medical Hello, I own a St Jude Medical that is covered by recall Z-2322-2018 from St Jude Medical. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
