Which COVID-19 Tests Were Recalled? A Comprehensive Guide

Which COVID-19 Tests Were Recalled? A Comprehensive Guide

The COVID-19 pandemic has brought about a surge in the development and usage of various diagnostic tests to detect the virus. While these tests have been crucial in combating the spread of the disease, some have been recalled due to various reasons such as false results, manufacturing defects, or lack of regulatory approvals. In this article, we’ll delve into the COVID-19 tests that have been recalled, the reasons behind their recall, and what it means for the public.

1. Roche’s Elecsys Anti-SARS-CoV-2 S1/S2 Antibody Test

In July 2020, Roche Holding AG recalled its Elecsys Anti-SARS-CoV-2 S1/S2 Antibody Test due to false positive results. The test, which detects antibodies against the COVID-19 virus, was found to produce false positive readings in some cases, leading to unnecessary concern and further testing.

2. Quidel’s Sofia 2 SARS Antigen FIA

Quidel Corporation recalled its Sofia 2 SARS Antigen FIA test in October 2020 due to concerns over false negative results. The test, which detects the virus’s antigens, was found to miss some cases of COVID-19, leading to delayed diagnosis and potential transmission of the virus.

3. BD Verrive SARS-CoV-2 Antigen Test

In February 2021, Becton, Dickinson and Company (BD) recalled its VerriVe SARS-CoV-2 Antigen Test due to manufacturing defects. The test, which detects the virus’s antigens, was found to produce inaccurate results, including false negatives, due to issues with the test’s packaging and labeling.

4. Abbott’s ID Now COVID-19 Rapid Test

Abbott Laboratories recalled its ID Now COVID-19 Rapid Test in February 2021 due to concerns over false positive results. The test, which detects the virus’s RNA, was found to produce false positive readings in some cases, leading to unnecessary concern and further testing.

5. BioMérieux’s Platelia SARS-CoV-2 Serology Test

In March 2021, BioMérieux recalled its Platelia SARS-CoV-2 Serology Test due to issues with the test’s calibration and quality control. The test, which detects antibodies against the COVID-19 virus, was found to produce inaccurate results, including false positives and false negatives.

What Does This Mean for the Public?

The recall of these COVID-19 tests is a significant concern, as it can lead to delayed diagnosis, unnecessary worry, and potential transmission of the virus. The public should be aware of the following:

  • If you have taken one of these recalled tests, you should contact your healthcare provider to discuss further testing and next steps.
  • If you are unsure about the test you took, you should contact the manufacturer or your healthcare provider to confirm the test’s accuracy.
  • Always follow proper testing protocols and guidelines, and consult with your healthcare provider if you have any concerns about COVID-19 testing.

Conclusion

The recall of COVID-19 tests is an important reminder of the importance of robust testing protocols and quality control measures. As new COVID-19 tests are developed and made available, it is essential to stay informed about any recalls or issues with these tests. By doing so, we can ensure the accuracy and reliability of COVID-19 testing, ultimately helping to combat the spread of the virus.