www.fgks.org   »   [go: up one dir, main page]

Please help us continue to provide you with free, quality journalism by turning off your ad blocker on our site.

For instructions on how to disable your ad blocker, click here.

I’ve Turned Off My Ad Blocker
BETA
This is a BETA experience. You may opt-out by clicking here
Edit Story
Editors' Pick|

Abbott Labs Eclipses 1.4 Million Rapid Coronavirus Tests Shipped Across U.S.

Bruce Japsen

Abbott Laboratories has shipped 1.4 million of its highly touted “rapid” molecular tests for the Coronavirus strain COVID-19 in the last month across the U.S., keeping ahead of its commitments to ramp up production.

The ability of Abbott to increase production and distribution of its ID NOW COVID-19 test is significant because it has been hailed in the ability of states across the U.S. to ramp up testing and re-open their economies. Abbott’s ID NOW COVID-19 test can deliver “positive results in as little as five minutes and negative results in 13 minutes.”

“We have shipped nearly 1.4 million of our rapid ID NOW tests to all 50 states, Washington D.C., Puerto Rico and the Pacific Islands,” Abbott said in an update posted on the company’s website Monday night. “The majority of these tests have been sent to outbreak hotspots and we've asked that customers prioritize frontline health care workers and first responders. We're currently manufacturing 50,000 tests per day, plan to increase ID NOW manufacturing capacity to 2 million tests a month by June and are working to expand beyond that.”

The test is regularly touted by President Trump as well as governors that are ramping up testing in their states. The Trump administration has been criticized for the availability of testing, which White House officials say is improving even with more than 1.1 million Coronavirus cases - the most reported from any country as of Tuesday morning.

Abbott’s ID NOW was granted the U.S Food and Drug Administration’s “emergency use authorization” at the end of March amid a growing number of agency approvals for more rapid molecular “point-of-care” diagnostic tests that can be used in temporary screening locations, doctor’s office labs and nursing homes to detect the Coronavirus strain COVID-19 within a half hour.

The FDA has escalated approvals of rapid “point-of-care” diagnostics made by other companies as well including Mesa Biotech, which has been shipping thousands of tests a week, and Cepheid which is also ramping up production to meet unprecedented demand.

Full coverage and live updates on the Coronavirus

Follow me on Twitter or LinkedInCheck out my website or some of my other work here

I've written about health care for three decades, starting from my native Iowa where I covered the presidential campaign bus rides of Bill and Hillary Clinton through the

I've written about health care for three decades, starting from my native Iowa where I covered the presidential campaign bus rides of Bill and Hillary Clinton through the Hawkeye state talking health reform and the economy. I have covered the rise, fall and rise again of health reform, chronicling national trends as well as the influence of Barack and Michelle Obama from Chicago's South Side on changes to the U.S. health system from my base in Chicago. I am the author of the book, "Inside Obamacare." A regular on Forbes on Fox (2014-2018), you can see me on occasion nationally on Fox Business News. In Chicago, you can hear my health segments and business analysis on WBBM News Radio 780 and 105.9 FM. I've written for many media outlets, including the New York Times (2011-2013) and was healthcare reporter at the Chicago Tribune (1998-2011). Prior to that, I wrote for Modern Healthcare and several Iowa newspapers including the Des Moines Register. I'm active in education and teach in the University of Iowa School of Journalism MA in Strategic Communication program. I am passionate about health literacy when it comes to explaining the complexities of health care. A better understood health system may save someone some money or their life.