Recall issued for popular nasal medicine sold at Walgreens, H-E-B and Amazon
The FDA recently announced a voluntary recall of a popular Sinu Cleanse nasal spray sold at retailers like H-E-B, Walgreens, ...
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No Doctor Needed: FDA Greenlights Self-Administered Flu Vaccine
This nasal spray vaccine can be self-administered or given by a caregiver, potentially increasing vaccination rates and ...
Nasal spray recalled nationwide; risk of infection: FDA
The U.S. Food & Drug Administration (FDA) has announced the voluntary recall of a sinus nasal wash bottle system following a ...
Nasal spray recalled for 'potentially life-threatening' bacterial contamination
The Food and Drug Administration issued a recall for certain nasal spray that tested positive for a bacterial contaminate ...
Nasal wash sold at Walmart and Amazon recalled for potentially causing ‘life-threatening infection,’ throw out ASAP
A nasal wash brand is being recalled due to contamination that could put you at risk for a life-threatening bacterial infection ...
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Nasal Wash Recalled Nationwide Over Staph Infection Risk
A batch of SinuCleanse nasal wash has been recalled after a test confirmed the presence of Staphylococcus aureus, a bacteria ...
Stop using this nasal wash sold nationwide immediately: It’s recalled for life-threatening risk, FDA warns
Nasal wash sold nationwide is being recalled at the consumer level, because it may cause serious and potentially ...
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FDA cancels advisory committee meeting on flu vaccine strain selection
VRBPAC members were alerted that the meeting was canceled in an email from the FDA that did not include an explanation, ...
5 recalls you should be aware of this week
Many recalls come as a result of product mislabeling, safety issues or contamination. Here are five recalls in particular ...
Nearly 100,000 bottles of nasal spray recalled for 'microbial failure'
Almost 100,000 bottles of nasal spray were recalled for a "microbial failure" that led to multiple complaints from customers.
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FDA Drug Approval Decisions Expected in March 2025
The Prescription Drug User Fee Act (PDUFA) date refers to the deadline set by the US Food and Drug Administration (FDA) for reviewing a New Drug Application (NDA) or Biologics License Application (BLA ...