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Artificial Intelligence (AI): Multidisciplinary perspectives on emerging challenges, opportunities, and agenda for research, practice and policy

As far back as the industrial revolution, significant development in technical innovation has succeeded in transforming numerous manual tasks and processes that had been in existence for decades where humans had reached the limits of physical capacity. Artificial Intelligence (AI) offers this same transformative potential for the augmentation and potential replacement of human tasks and activities within a wide range of industrial, intellectual and social applications. The pace of change for this new AI technolo…

International Journal of Information Management · Policy

Artificial Intelligence (AI): Multidisciplinary perspectives on emerging challenges, opportunities, and agenda for research, practice and policy
Ossur H F Grjothals 5 Reykjavik Iceland recalls an AI-enabled medical device
Evidence-backed problem

Ossur H F Grjothals 5 Reykjavik Iceland recalls an AI-enabled medical device

The Rheo Knee bionic prosthetic is to be used exclusively for fittings of lower extremity amputations. RHEO KNEE uses Artificial Intelligence to continuously adapt to the users walking style and environment. The RHEO KNEE recognizes and responds immediately t… Recall reason: The firm is recalling Rheo Knee bionic prosthetic due to it being discovered during an internal audit of the service line that devices were released for distribution without fully going through the assembly process.

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Reveal linq: FDA malfunction report involving AI
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Reveal linq: FDA malfunction report involving AI

The FDA received a malfunction report involving Reveal linq, made by Medtronic europe sarl. It was reported that the implantable cardiac monitor (icm) experienced false pause episodes due to undersensing. it was reported that representative stated the customer is concerned that the artificial intelligence (ai) algorithm adjudicated some pause episodes as false when they determined to be true. the icm remains in the patient. no patient complications have been reported as a result of this event.

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Accurhythm za420 (pause): FDA malfunction report involving AI
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Accurhythm za420 (pause): FDA malfunction report involving AI

The FDA received a malfunction report involving Accurhythm za420 (pause), made by Medtronic, inc.. It was reported that true pause episodes were rejected as false by the artificial intelligence (ai) algorithm. no patient complications have been reported as a result of this event.

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Linq ii¿ insertable cardiac monitor: FDA malfunction report involving AI
Evidence-backed problem

Linq ii¿ insertable cardiac monitor: FDA malfunction report involving AI

The FDA received a malfunction report involving Linq ii¿ insertable cardiac monitor, made by Medtronic singapore operations. It was reported that true pause episodes were rejected as false by the artificial intelligence (ai) algorithm. it was further reported that the implantable cardiac monitor (icm) detected false ventricular tachycardia (vt) episodes. the icm remains in use. no patient complications have been reported as a result of this event.

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