Pediatric Septic Shock Therapies Perform Equally Well
Data on 9,000 children with septic shock shows no difference in kidney outcomes between two common types of IV fluids used for emergency resuscitation.
Data on 9,000 children with septic shock shows no difference in kidney outcomes between two common types of IV fluids used for emergency resuscitation.
Data on 9,000 children with septic shock shows no difference in kidney outcomes between two common types of IV fluids used for emergency resuscitation.
Read MoreGE HealthCare has issued a letter to affected customers recommending Infant Resuscitation Systems and Warmers with a M1091607-R blender be corrected prior to continued use, according to an FDA alert.
Read MoreA national parent poll reports gaps in community preparedness for teen cardiac emergencies and concerns about school readiness.
Read MoreZoll Medical’s Zenix monitor/defibrillator is now approved under the European Union’s Medical Device Regulation 2017/745, commonly referred to as EU MDR.
Read MoreThe CPR-2+ manual resuscitator features a 1,000 mL capacity and tidal volume markings to align with clinical guidelines and reduce ventilation injuries.
Read MoreThe Resp-O2 Manual Pulmonary Resuscitators feature a nonslip grip, preassembled tubing, and a swivel port to assist healthcare professionals during resuscitation.
Read MoreZoll has completed the US rollout of its next generation garment for the LifeVest wearable cardioverter defibrillator (WCD), according to the company.
Read MoreThe FDA issued import alerts and warning letters to companies marketing unauthorized anti-choking devices.
Read MoreNew guidelines from the AAP/AHA update procedures for pediatric and neonatal CPR and emergency cardiovascular care for the first time since 2020.
Read MoreZoll (an Asahi Kasei company) recently announced its Zenix monitor/defibrillator received premarket approval by the US FDA.
Read MoreBystander confidence to administer life-saving aid like CPR rises to almost 10% if real-time coaching is available, according to a Zoll survey.
Read MoreAmbu Inc is recalling Spur II manual resuscitators due to the manometer port being blocked, which renders the manometer non-functional, according to an FDA alert.
Read MoreCertain Boston Scientific Endotak Reliance Defibrillation leads with ePTFE coated coils may impact shock efficacy and/or require early replacement, according to an FDA alert.
Read MorePoisonings and deaths linked to the use of the local anesthetic lidocaine have nearly tripled in the US over the past decade, despite drops for in poisonings and deaths related to other anesthetics.
Read MoreSunMed recalled its Adult Manual Resuscitator devices due to incorrect assembly of the B/V filter, which may lead to delayed emergency therapy.
Read MoreRT’s 2025 Product Focus provides a detailed look at 68 of the newest medical devices, including 33 exclusive products not available in the print edition.
Read MoreThe FDA is reporting that Zoll has recalled its AutoPulse Nxt Resuscitation System due to a failure code that may cause the device to stop delivering chest compressions or fail to compress deeply enough, according to an FDA alert.
Read MoreRT looks at the latest resuscitation devices on the market from manufacturers like Dynarex, Flexicare, and Mercury Medical.
Read MoreResults from a national survey reveal a concerning gap in awareness and understanding about the role AEDs play in a cardiac emergency.
Read MoreThe American Heart Association and the Buffalo Bills started the HeartBeat initiative in 2023 to increase bystander CPR skills after Damar Hamlin suffered cardiac arrest during a game.
Read MoreNew data presented at ESC’s ACVC 2025 reveals that time to CPR initiation for out-of-hospital cardiac arrest (OHCA) is more critical to successful outcomes than who performs the CPR.
Read MoreOpusVi and Laerdal Medical will offer simulation training and validation of competencies through the use of high-fidelity simulation mobile laboratories.
Read MoreSuccess achieving a secure airway for difficult airway patients relies on the skills and knowledge of emergency medicine and critical care providers.
Read MoreMercury Medical is removing certain Neo-Tee T-Piece resuscitators from where they’re used or sold after a defect in the device’s controller was found to potentially prevent proper ventilation.
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