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Most pregnant women 🤰🏾 surveyed expressed a strong desire to breastfeed exclusively. However, a sustained flow of misleading marketing messages

Most pregnant women 🤰🏾 surveyed expressed a strong desire to breastfeed exclusively.

However, a sustained flow of misleading marketing messages reinforces myths about #breastfeeding & breast milk, undermining women’s confidence in their ability to breastfeed successfully. https://t.co/4EazCEPVqM

 
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Baxter recalls SIGMA Spectrum Infusion Pumps with Master Drug Library (Version 8) and Spectrum IQ Infusion Systems with Dose IQ Safety Software (Version 9) due to the risk of not alarming for repeated upstream occlusion events

There is a risk of the pumps not delivering medication at the programmed rate displayed on the screen, and in some cases may not alarm for upstream occlusions.

http://www.fda.gov/medical-devices/medical-device-recalls/baxter-recalls-sigma-spectrum-infusion-pumps-master-drug-library-version-8-and-spectrum-iq-infusion

 
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ACON Laboratories Issues a Recall of Non-EUA Authorized “Flowflex™ SARS-CoV-2 Antigen Rapid Test (Self-Testing)” Tests From the U.S. Market

ACON Laboratories, Inc. (“ACON Laboratories”), the legal manufacturer of the “Flowflex™ COVID-19 Antigen Home Test” (FDA Emergency Use Authorization EUA210494), has identified the U.S. distribution of unauthorized, adulterated and misbranded counterfeit product having the trade name “Flowflex SARS-C

http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/acon-laboratories-issues-recall-non-eua-authorized-flowflextm-sars-cov-2-antigen-rapid-test-self