Even peaceful protests can quickly devolve into violent events representing a life-safety risk to everyone in the environment, especially first responders tasked with crowd management and public safety. Whether working on the frontlines of a protest or staffing a Point of Dispensing (POD) during a public health emergency, all first responders can benefit from a working knowledge human behavior in group, crowd and mob situations.
The EMS Council of NJ announces the cancellation of its 2020 Symposium and Trade Show, originally scheduled for October.
If you made reservations at the Sheraton Parsippany Hotel you must call and Cancel them they are not automatically canceled. (973) 515-2000 or Call 888-627-8148 to Cancel by phone
This difficult decision was made due to the ongoing concerns with the Covid-19 Pandemic. This is the first time in the 91-year history of the Council that a Convention was cancelled, but be assured that we will be back next year with a bigger and better convention.
Thank you to the convention committee for all the time they had already put into planning this event. We also thank our loyal supporters, our vendors, instructors, the Sheraton Hotel and many attendees for your continued support. It is greatly appreciated.
The officers of the organization are looking into an alternate plan for our business meeting so the members can participate in the business of the Council.
In light of recent incidents in the news, the White House has released guidelines and safe practices to deal with the growing concern of illicit use of the opiod drug FENTANYL when responding to emergency calls. Use the links below for the poster and further details:
To all users of PHYSIO-CONTROL LIFEPAK EXPRESS®, CR®, Plus AED, Model 1000 and Model 500 BiPhasic AEDs: There is a voluntary recall of specific production lots of Infant/Child defibrillation electrodes produced by Cardinal Health. Your attention to this recall is required.
ISSUE: Mylan N.V. announced that Meridian Medical Technologies, a Pfizer company and Mylan’s manufacturing partner for EpiPen Auto-Injector, has expanded a voluntary recall of select lots of EpiPen (epinephrine injection, USP) and EpiPen Jr (epinephrine injection, USP) Auto-Injectors to now include additional lots distributed in the U.S. and other markets.
The Food and Drug Administration (FDA) on January 14 issued a Safety Alert announcing the voluntary field action by Physio-Control (Redmond, Washington) notifying its customers to immediately remove and reinstall batteries in the Lifepak 1000 defibrillator.
The company has received 34 reports of customers attempting to use the defibrillator, and the device shut down unexpectedly because of an intermittent connection between the battery and device electrical contacts. The intermittent connection is a result of wear and subsequent oxidation formation between the battery and electrical contacts, according to the company.
Physio-Control is aware of 8 adverse events related to this issue.
Nurse Assist, Inc. announced this week that it is voluntarily recalling all unexpired lots of I.V. Flush Syringes due to a potential link to Burkholderia cepacia bloodstream infections with the product. According to the U.S. Centers for Disease Control and Prevention (CDC), the effects of Burkholderia cepacia on people "vary widely, ranging from no symptoms at all to serious respiratory infections, especially in patients with cystic fibrosis." If a patient is having symptoms, contact your health care provider.
Product Numbers 1203 (3 ml syringe), 1205 (5 ml syringe), and 1210 (10 ml syringe) are packaged 30 syringes to an inner carton and six inner cartons in a case (180 syringes). For product number 1210-BP (10 ml syringe), 100 syringes are packaged in an inner carton with four inner cartons in a case (400 syringes). Lot code information can be found on the outer case panel, the back panel of the inner carton, and on each syringe label.
The lots being recalled were distributed to customers and distributors between 02/16/16 and 09/30/16. Product can be identified by the labeling on the packaging and device. Nurse Assist is directing customers not to use the product from recalled lots. Recalled product should be returned for credit by contacting Nurse Assist Customer Service at 1-800-649-6800 ext. 10, Monday through Friday, between the hours of 8am and 5pm, Central Time.
Nurse Assist voluntarily recalled its I.V. Flush Syringes after becoming aware of patients that developed Burkholderia cepacia bloodstream infections while receiving intravenous care using prepackaged saline flushes from Nurse Assist
Nurse Assist is notifying its distributors and customers via email, phone call, and certified mail. Customers will receive instructions for returning product. For freight collect shipping information, please contact the Customer Service Team at 1-800-649-6800 ext. 10.
Nurse Assist is actively investigating the possible link to the infections with the Food and Drug Administration, the U.S. Centers for Disease Control, and various state health departments to ensure that the products are safe for their intended use. Until an investigation can be completed, Nurse Assist urges all healthcare facilities with affected product to discontinue use and return the product to the supplier.
Consumers with questions may contact the company via telephone at 1-800-649-6800 ext. 10, Monday through Friday, between the hours of 8am and 5pm, Central Time. Consumers may also contact the company via email at ProductRemovalInfo@nurseassist.com.
Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA's MedWatch Adverse Event Reporting program either online, by regular mail or by fax.