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Risk Managers and Biomedical Engineers are informed by the FDA that Giraffe OmniBed and Giraffe Incubator are recalled because there is a potential of a malfunction if the device randomly deletes stored information when powered on. This may pose a serious health risk to newborn babies. Background of Giraffe OmniBed and Giraffe Incubator The Giraffe [...]

Risk Manager and Healthcare Professionals are informed by the FDA that HeartSine Samaritan Public Access Defibrillator 300/300P is recalled because certain devices may intermittently turn on and off and may eventually deplete the battery being unable to deliver therapy. Background of HeartSine Samaritan Public Access Defibrillator 300/300P Samaritan 300/300P PAD devices, by HeartSine Technologies Limited, [...]

Risk Manager, Pharmacy and Family Practice healthcare professionals are informed by the FDA that Citalopram and Finasteride by Greenstone are recalled because there is a possibility of mislabeling. Background of Citalopram and Finasteride by Greenstone Citalopram, by Greenstone LLC, is used to treat depression and Finasteride is used for the treatment of benign prostatic hyperplasia. [...]

Risk Manager and Critical Care Medicine personnel are informed by the FDA that CareFusion Alaris PC Unit, Model 8015 is recalled because an error code may result in serious injury, including death. Background of CareFusion Alaris PC Unit, Model 8015 Alaris PC Unit, Model 8015, by CareFusion 303 Inc, is part of the Alaris electronic [...]