Innova Medical Group Recalls Unauthorized Sars Cov 2 Antigen Rapid Qualitative Test Risk False Test

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The FDA has identified this as a Class I recall, the most serious type of recall. Use of these devices may cause serious injuries or death.
READ HERE: US Food and Drug Administration:
The FDA has identified this as a Class I recall, the most serious type of recall. Use of these devices may cause serious injuries or death.
READ HERE: US Food and Drug Administration:

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