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The FDA has extended the shelf life of nearly 1 million rapid COVID-19 test kits that first expired in a Florida warehouse in September, the Miami Herald reported Jan. 11. 

Medical device recalls, whether voluntary or mandated by the FDA, ensure patient safety. 

The increasing demand for COVID-19 testing is prompting some labs across the U.S. to ration access and prioritize patients presenting symptoms or other health concerns, The Wall Street Journal reported Jan. 10.

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