St Jude Medical is a leading manufacturer of medical devices, including pacemakers, defibrillators, and other cardiac devices.
New pacemaker firmware was developed to further mitigate the risk of unauthorized access to our pacemakers that utilize radio frequency (RF) communications.
St Jude Medical is a well-known company that specializes in the design, manufacturing, and distribution of medical devices, particularly cardiac devices such as pacemakers and defibrillators. They are a leader in the medical device industry and have a strong reputation for innovation and quality.
The company is a legitimate medical device manufacturer with a strong reputation for safety and quality. There are no known safety risks associated with St Jude Medical products.
Patients with cardiac devices (pacemakers, defibrillators), healthcare professionals, and the general public
Check for proper medical device certifications (e.g., FDA approval), ensure the device is functioning correctly, and follow the manufacturer's instructions for use and maintenance.
Ensure the device is properly implanted and functioning as intended by a qualified medical professional.
Regularly monitor the device's performance through scheduled check-ups with your healthcare provider.
Follow the manufacturer's guidelines for device maintenance and battery replacement.
Yes, St Jude Medical is a reputable company with a strong safety record. Their devices undergo rigorous testing and are approved by regulatory bodies like the FDA.
It is recommended to have your device checked at least once a year by a healthcare professional, or as per your doctor's instructions.
No, battery replacement should only be performed by a qualified medical professional to avoid risks such as infection or device malfunction.
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-0031-2018 — St Jude Medical St Jude Medical Hello, I own a St Jude Medical that is covered by recall Z-0031-2018 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.
