Boston Scientific Recalls ACCOLADE EL DR Pacemakers for Sensor Issues
Boston Scientific is recalling ACCOLADE EL DR pacemakers due to reports of intermittent over-sensing of the Minute Ventilation sensor signal.
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 medical device with a functional defect (sensor over-sensing) that poses a risk of harm, but the source text does not report any specific injuries, illnesses, or fatalities, aligning with the 'High' severity criteria for risk-of-harm products where injury has not yet been reported.
Plain-English summary
Boston Scientific Corporation is recalling ACCOLADE EL DR Pacemakers (Model L321) due to reports of intermittent over-sensing of the Minute Ventilation (MV) sensor signal. This issue affects certain Boston Scientific pacemaker and cardiac resynchronization therapy pacemaker systems.
The recall covers devices distributed across all 50 U.S. states, Puerto Rico, and worldwide. The source text does not specify the total number of units affected or the specific dates of distribution.
Consumers with these devices should contact their healthcare provider or Boston Scientific for further instructions on how to address the sensor signal issue.
The recalled product
- Product
- ACCOLADE EL DR Pacemaker
- Manufacturer
- Boston Scientific Corporation
- Category
- Medical Device — Pacemaker
- Hazard
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (1)
- Model L321
Distribution
Part of a larger recall action
This product is one of 24 recalled by Boston Scientific Corporation 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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