![]() A former hospital administrator and nurse, Kim self-medicated at first until she realized what she felt was more than a minor pain. Whether she was giving her time at the nursing home or church, playing golf, swimming, oil painting, or gardening, Kim was “constantly doing something.” But things changed for her in January 2003 when she felt an unusual pain in her back while playing golf. More details on the recall are available from the FDA.Kim considered herself a “professional volunteer” in her retirement. The FDA approved Abbott’s Patient Controller smartphone app in 2020. Abbott has distributed a physician communication to reinforce the importance of following the steps regarding MRI scans outlined in the IFU.” “Based on these occurrences, Abbott previously updated the patient controller Instructions for Use (IFU) and patient controller application MRI-mode screen on smartphones reminding the patient to not delete the paired Bluetooth connection between their Implantable Pulse Generator (IPG) and the patient controller. “Abbott has received reports indicating the loss of Bluetooth connectivity between Abbott’s implantable Proclaim and Infinity systems and its paired patient controller after a patient has undergone an MRI,” the company said.
0 Comments
Leave a Reply. |
AuthorWrite something about yourself. No need to be fancy, just an overview. ArchivesCategories |