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U.S. Department of Health and Human Services

Medical Device Recalls
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Z-1299-2021 - The ImmunoCard Mycoplasma EIA detects the presence of IgM to M. pneumoniae in serum - Product Usage: intended to aid in the diagnosis of recent Mycoplasma pneumoniae infection. 2 03/24/2021 FEI # 1524213
Meridian Bioscience Inc
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