FDA Says Medtronic Reports 28 Complaints Related To StealthStation S8 Application Issue; Medtronic Recalled Certain StealthStation S8 Application Versions For Software Error That May Cause Incorrect Measurements During Cranial Surgery
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Medtronic has reported 28 complaints related to an issue with its StealthStation S8 application, which has led to a recall of certain versions of the software due to a potential error that may cause incorrect measurements during cranial surgery.
June 05, 2024 | 3:15 pm
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Medtronic has recalled certain versions of its StealthStation S8 application due to a software error that may cause incorrect measurements during cranial surgery. The FDA has reported 28 complaints related to this issue.
The recall of a medical device due to software errors, especially one used in critical procedures like cranial surgery, is likely to negatively impact Medtronic's stock in the short term. The 28 complaints reported to the FDA highlight the severity of the issue.
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