St Jude Medical Recalls Quadra Assura MP Implantable Cardiac Devices for Security Update
St Jude Medical is recalling 68,117 Quadra Assura MP implantable cardiac devices to release new firmware that strengthens security against unauthorized access.
What this means for you
Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.
Our severity reasoning: The recall involves a risk-of-harm product (implantable cardiac device) with a security vulnerability that could allow unauthorized access, but no injuries or illnesses have been reported.
Plain-English summary
St Jude Medical Inc. is recalling 68,117 units of the Quadra Assura MP, Sterile EO, implantable cardiac devices (ICD) and cardiac resynchronization therapy defibrillators (CRT-D). The recall is being conducted to release new firmware intended to strengthen security by providing an additional layer of protection against unauthorized device access.
The affected devices were distributed nationwide in the United States. For older generation devices that are not capable of accepting the new firmware, the firm is advising customers of the option to permanently disable the RF communication capability in these devices.
The recalled product
- Product
- Quadra Assura MP, Sterile EO, Model #/ Part #: CD3269-40/100043177; CD3269-40Q/100043178; CD3271-40/100043130; CD3271-40Q/100043191; CD3369-40C/100080339, 100080478; CD3369-40Q/100080439, 100080476, 100105528; CD3371-40/100078814, 100079232, 100079513; CD3371-40C/
- Manufacturer
- St Jude Medical Inc.
- Affected units
- 68,117
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 12 recalled by St Jude Medical Inc. under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
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