It's a Class I recall, the most serious kind there is.
According to the FDA, the company initially contacted customers who may have been impacted by the recall by phone between March 4 and March 12. Subsequently, on March 21, the firm followed up with emails to each affected distributor with subject line"IMPORTANT!!! Recall Notice" and a recall letter attachment.
Customers were asked by the company to immediately return all unused product, and were sent another email on March 25 which instructed them to not rely on the recalled tests for medical decisions, the FDA said.Test users and caregivers should talk to their health care provider if they tested with the Skippack Medical Lab SARS-CoV-2 Antigen Rapid Test and you have concerns about test results.are advised by the FDA to reconsider testing patients with an FDA-authorized test if they were initially tested with the Skippack Medical Lab SARS-CoV-2 Antigen Rapid Test in the last 2 weeks and you suspect an inaccurate result.
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