St Jude Medical Inc. is a leading manufacturer of medical devices and products. Explore their product catalog for the latest innovations in cardiac care and more.
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 Inc. is a leading manufacturer of medical devices and products, specializing in cardiac care solutions. Their product catalog includes a wide range of devices for cardiac procedures, including pacemakers, defibrillators, and other critical medical equipment.
Low risk due to the company's focus on medical device safety and regulatory compliance
Patients, healthcare providers, and medical facilities using St Jude Medical products
Check for product-specific safety guidelines and proper usage instructions
Ensure you have the correct product model and version before use.
Consult the manufacturer's safety guidelines for the specific product.
Confirm that healthcare providers have received appropriate training for the product.
St Jude Medical Inc. is a leading manufacturer of medical devices and products, specializing in cardiac care solutions.
Yes, St Jude Medical products undergo rigorous safety testing and regulatory compliance checks.
Follow the product-specific safety guidelines and ensure healthcare providers have received appropriate training.
We’ve drafted a message you can send St Jude Medical Inc. to request your refund or repair — edit it as you like.
Subject: Recall Z-2318-2018 — St Jude Medical Inc. St Jude Medical Inc. Hello, I own a St Jude Medical Inc. that is covered by recall Z-2318-2018 from St Jude Medical Inc.. 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.
