Boston Scientific Recalls ACCOLADE DR Pacemakers Due to Sensor Issues
Boston Scientific is recalling ACCOLADE DR pacemakers because the Minute Ventilation sensor may intermittently over-sense signals.
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 is classified as FDA Class II. The hazard involves a sensor malfunction in a medical device where injury has not yet been reported, fitting the 'High' severity criteria for risk-of-harm products.
Plain-English summary
Boston Scientific Corporation is recalling ACCOLADE DR Pacemakers. The recall involves Model L301 devices.
The recall is being conducted because Boston Scientific has received 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 affected devices were distributed in all 50 U.S. states, Puerto Rico, and worldwide. Consumers with these devices should contact their healthcare provider or Boston Scientific for further instructions.
The recalled product
- Product
- ACCOLADE 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 L301
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.
See all 24 products in this recall →Related recalls
Same manufacturer · Boston Scientific Corporation
See all →- HighBoston Scientific Recalls Suture Cinch Endoscopic Tissue Approximation Devices
FDA (Devices) · 2026-08-26
- HighBoston Scientific ENROUTE Transcarotid Neuroprotection System Plus Recall
FDA (Devices) · 2026-08-26
- HighBoston Scientific Recalls OverStitch Suture Cinch Devices for Deployment Failure
FDA (Devices) · 2026-08-26
- HighBoston Scientific ENROUTE Transcarotid Neuroprotection System Recall for Tip Separation
FDA (Devices) · 2026-08-26
- SevereRadial Jaw 4 Jumbo Biopsy Forceps Packaging Sterile Barrier Recall
FDA (Devices) · 2026-08-12
Same hazard · sensor malfunction
See all →- ModeratePhotera 600 3-D phototherapy device UV sensor calibration error recall
FDA (Devices) · 2026-07-22
- ModeratePhotera 600 Phototherapy Device UV Sensor Calibration Error
FDA (Devices) · 2026-07-22
- SevereiLet Bionic Pancreas Software Versions Recalled for Delayed CGM Readings
FDA (Devices) · 2026-05-06
- SevereAbiomed Impella RP with SmartAssist recalled as Class I
FDA (Devices) · 2026-03-11
- SevereAbiomed Impella RP recalled as Class I over sensor malfunction risk
FDA (Devices) · 2026-03-11