Boston Scientific StoneSmart Connect Console Power Adapter Recall
Boston Scientific is recalling StoneSmart Connect Console power adapters that may fail electrical safety testing due to high grounding resistance.
What this means for you
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: The recall is classified as FDA Class II, and the hazard involves a potential failure of electrical safety testing during installation without reported injuries, fitting the criteria for a moderate severity recall.
Plain-English summary
Boston Scientific Corporation is recalling a subset of power adapters used with the StoneSmart Connect Console. The recall involves 982 units distributed worldwide, including nationwide distribution in the United States and in various international countries.
The power adapters are being recalled because they may exhibit higher-than-expected resistance in the electrical grounding path. As a result, the power adaptor may fail electrical safety testing during installation.
The source text does not specify specific actions for consumers or healthcare facilities, nor does it report any injuries or illnesses associated with the product.
The recalled product
- Product
- Boston Scientific Corporation StoneSmart Connect Console Contents: (1) Power Cord, (1) Power Adaptor, (1)DVI Cable, (1) DVI to HDMI Cable, (1) DisplayPort Cable REF: M0067933000, M006793300H0, M006793300R0, M006793300D0, M006793300Z0, M0067930000, M006793000R0
- Manufacturer
- Boston Scientific Corporation
- Category
- Medical Device — Power Adapter
- Affected units
- 982
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 (8)
- All Serial Numbers: REF: M0067933000 (UDI 00191506002510
- UDI (00191506021771)
- REF: M006793300H0 (UDI 00191506002558)
- REF: M006793300R0 (UDI 00191506002534)
- UDI (00191506021788)
- REF: M006793300D0 (UDI 00191506002527)
- REF: M006793300Z0 (UDI 00191506002541)
- UPN M0067933100 (UDI 00191506022549)
Distribution
Related recalls
Same manufacturer · Boston Scientific Corporation
See all →- HighBoston Scientific Recalls LUX-Dx Insertable Cardiac Monitor Server Software
FDA (Devices) · 2026-09-09
- HighBoston Scientific Recalls LUX-Dx Insertable Cardiac Monitor Server Software
FDA (Devices) · 2026-09-09
- HighBoston Scientific Recalls LUX-Dx Insertable Cardiac Monitor Server Software
FDA (Devices) · 2026-09-09
- 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
Same hazard · electrical safety failure
See all →- HighRecalled CLARAVUE Pre-wired Electrode Set May Fail During Defibrillation
FDA (Devices) · 2022-04-20
Similar recalls
- ModerateBoston Scientific reusable CSK stainless steel electrodes may underperform expected levels
FDA (Devices) · 2026-06-17
- HighPhilips Recalls Speaker Power Adapters Sold With HP Computers
CPSC · 2002-05-16
- HighBoston Scientific ROTAPRO System Console Recalled for Manufacturing Instruction Deficiency
FDA (Devices) · 2021-12-22
- HighBoston Scientific Recalls One Step Button PEG Kits Due to Adapter Defect
FDA (Devices) · 2015-12-16
- LowBoston Scientific Recalls Spinal Cord Stimulation Leads Due to Labeling Error
FDA (Devices) · 2020-06-03
- HighSonitrol Connector Kits Recalled Due to Entrapment Hazard
CPSC · 2010-01-21