Spark Biomedical Inc has recalled 78 Sparrow Ascent Patient Controllers (various models) due to a manufacturing defect. This issue can cause a "cable disconnect" error message, which stops the device from delivering its intended neurostimulation therapy. Consumers should stop using the affected controllers and contact their healthcare provider or the manufacturer to arrange for a return or replacement.
The manufacturing defect causes the device to stop delivering stimulation therapy unexpectedly. This interruption can lead to a loss of therapeutic benefit and the potential return of symptoms for the patient.
Manufacturing issue causes "cable disconnect" error message.
If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.
This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.
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Sources: FDA iRES · Raw API Response
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