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‘Rural Medical Club’ posts a lot to keep an eye on 8.5 million ATK sets that the Government Pharmaceutical Organization has not purchased as standard. pointed out that it could be catastrophic

12 Aug 2021 Rural Medical Club Posted via Facebook said that the Government Pharmaceutical Organization to buy ATK, even if it is the lowest price. A low quality ATK is a disaster that will destroy confidence in ATK in diagnosing COVID.
The Pharmaceutical Organization (GPO) has announced that has purchased 8.5 million ATK test kits that the company has been Expedite delivery to the NHSO before the end of August

However, the brand chosen by the Pharmaceutical Organization is the Lepu brand. On May 28, 2021, the US FDA has announced a recall of Lepu Medical Technology SARS-CoV-2 Antigen Test and Antibody Test named Lecurate Antibody Test. of a manufacturer named Lepu Medical Technology, a product from China due to problems with fake test results It is at a high risk to the user (performance of the test likely a high risk of false negative).

The United States FDA or FDA does not authorize, pass, or approve both tests for distribution or use in the United States. but in Thailand The Pharmaceutical Organization is about to order 8.5 million kits during the severe coronavirus outbreak. New infections soar 20,000 cases per day

For the Antibody Rapid Test Kit Leccurate SARS-CoV-2 (Colloidal Gold Immunochromatography) Healthcare Providers. Consider re-examination with another antibody test if past infection is suspected. The testers and supervisors Talk to your health care provider if you are concerned about the possibility of testing with the Leccurate SARS-CoV-2 Antibody Rapid Test Kit (Colloidal Gold Immunochromatography) and concerned about the results. and report any problems arising from the use of the Leccurate SARS-CoV-2 Antibody Rapid Test Kit (Colloidal Gold Immunochromatography) to the FDA, including any suspected inaccuracies.

The FDA is deeply concerned about the efficacy of Lepu Medical Technology’s Antigen Rapid Test Kit and believes there is a high likelihood of false results when using this test. Have passed or approved by the FDA to distribute this test kit.

same day On its website, the FDA announced that Lepu Medical Technology is recalling both the Antigen Rapid Test Kit and the Antibody Rapid Test Kit due to the risk of fake test results. 1(Class I recall), which is the most serious type of recall. Using these devices can result in serious injury or death.

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