ihealth covid test expiration date extension

"That was a little disappointing, just given that theres this new Covid variant going around and cases are continuing to go up. September 6, 2022: FDA and HHS/ASPR authorized an extension to the shelf life from 12 months to 18 months for certain lots of the Pfizer antiviral therapy, Paxlovid (nirmatrelvir tablets and ritonavir tablets co-packaged for oral use). Brands . However, when enforcement discretion is used for medical product dating extensions, MCMs are not covered under applicable Public Readiness and Emergency Preparedness (PREP) Act liability protections. The FDA granted another three-month shelf-life extension for the iHealth COVID-19 Antigen Rapid Test, which extended the shelf-life of all iHealth tests with expiration dates on or before 2022-09-29 (YYYY-MM-DD) 6 months from the date on the box. PAHPRA provides FDA with the explicit authority to extend the expiration dating of eligible FDA-approved MCMs stockpiled for use in CBRN emergencies. Back to school, back to the office, or just back from travel or public gatherings, a rapid,15-minute, self-test is waiting at home for when you get back. In late March, the FDA granted a three-month extension past the expiration dates for the iHealth brand of COVID-19 antigen rapid tests. Insert the swab with the sample into the bottom of the tube and stir it in the fluid 15 times. The other two tests expire in a month. This is not a PCR test and not valid for travel. Please see the most recent updates above for the latest information. That means if your free iHealth rapid test has a "use by" date April, the new date has been extended to July, as long as it has been stored between 2 and 30 degrees Celsius (35.6 and 86 . Update: The iHealth COVID-19 Antigen Rapid Test shelf life has increased by 3 months. But the boxes have already been distributed, with the original expiration date already listed on it.. Also see: Expiration date extensions of certain lots of doxycycline hyclate. If theres liquid in the test, it can potentially evaporate over time, which means you wont have enough liquid volume to properly conduct the test. Due to the high frequency of the omicron variant and its subvariants, REGEN-COV is not currently authorized in any U.S. region. QuickVue At-Home OTC COVID-19 Test (Quidel Corporation), InteliSwab COVID-19 Rapid Test (OraSure Technologies, Inc.), OHC COVID-19 Antigen Self Test (Osang LLC), (This test is manufactured by ACON Laboratories under the name "Flowflex."). (Your test may look different.) Please refer to the table on this page for updates. This posting and memorandum replace FDAs March 23, 2018, posting and all previous FDA web postings and memoranda notifying health care professionals and emergency responders about the expiration dating of such auto-injectors.