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The FDA informs Pharmacists, Patients and healthcare professionals that Carboplatin Injection is recalled due to visible particulates identified as Carboplatin crystals that may cause vasculitis, local infarction and thromboembolism. Background of Carboplatin Injection Carboplatin Injection, by Hospira Inc., is indicated for the initial treatment of advanced ovarian carcinoma in established combination with other approved chemotherapeutic [...]

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, [...]

The FDA informs Risk Managers and Healthcare Professionals that Ameridose unexpired products are recalled because there are concerns about a lack of sterility assurance for these products. Use on non-sterile products can lead to life-threatening consequences. Background of Ameridose Unexpired Products A complete list of the recalled products by Ameridose LLC can be found at [...]

[update] The FDA notifies healthcare professionals that Stryker Neptune Rover Waste Management Systems are recalled. The affected products are: Neptune 2 Rover Ultra (120V), Neptune 2 Rover Ultra (230V), Neptune 1 Gold Rover (120V), Neptune 1 Gold Rover International (230V), Neptune 1 Silver Rover (120V) and Neptune 1 Bronze Rover. The affected products were manufactured [...]