The National Institute for Occupational Safety and Health today revoked its public health certificate of approval for Plastikon Industries’ PLASMA N95-01 filtering facepiece respirator for failure to meet filter efficiency requirements in a product audit. Effective April 8, the respirator is no longer NIOSH-approved and may no longer be manufactured, assembled, sold or distributed, the agency said.

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The Department of Health and Human Services Sept. 18 announced the launch of a new personal protective equipment forecast to identify, consolidate and publish…
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The Centers for Medicare & Medicaid Services Jan. 26 released an advanced notice of proposed rulemaking seeking comments on potential future policies to…
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The Food and Drug Administration Nov. 9 cleared for marketing the Flowflex COVID-19 Antigen Home Test, the first COVID-19 antigen test and second COVID-19 at-…
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The Department of Health and Human Services’ Administration for Strategic Preparedness and Response yesterday awarded $600 million for 12 domestic COVID-19…
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The National Institute for Occupational Safety and Health this week revoked eight N95 filtering facepiece respirator approvals and four powered air-…
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In response to questions from AHA and others and informed by testing results, the Food and Drug Administration April 21 announced that health care…