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Safety Recall for Deluxe Heat Therapy Massager
Wahl Clipper Corporation is voluntarily recalling all Deluxe Heat Therapy Massagers, Model 4212.
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Meitheal Pharmaceuticals, Inc. Issues Voluntary Nationwide Recall of Cisatracurium Besylate Injection, USP 10mg per 5mL Due to Mislabeling
Meitheal Pharmaceuticals, Inc. (“Meitheal”), announced today that it is voluntarily recalling one (1) lot of Cisatracurium Besylate Injection, USP 10mg per 5mL to the user level. The decision to recall the product was made after a product complaint revealed that a portion of Lot C11507A of cartons l
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Coronavirus (COVID-19) Update: January 26, 2021
Coronavirus (COVID-19) Update: January 26, 2021
http://www.fda.gov/news-events/press-announcements/coronavirus-covid-19-update-january-26-2021
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País suma 831 casos COVID-19 el viernes, 651 el sábado, 431 el domingo, 355 el lunes y 600 hoy martes: 191.341 casos COVID-19 totales
País suma 831 casos COVID-19 el viernes, 651 el sábado, 431 el domingo, 355 el lunes y 600 hoy martes: 191.341 casos COVID-19 totales
Martes 26 de enero, 2021. El país registró 831 casos nuevos de COVID-19 el viernes 22 de enero, 651 el sábado 23 de enero, 431 el domingo 24 de enero…
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Coronavirus (COVID-19) Update: FDA Takes Action to Place All Alcohol-Based Hand Sanitizers from Mexico on Import Alert to Help Prevent Entry of Violative and Potentially Dangerous Products into U.S., Protect U.S. Consumers
Coronavirus (COVID-19) Update: FDA Takes Action to Place All Alcohol-Based Hand Sanitizers from Mexico on Import Alert to Help Prevent Entry of Violative and Potentially Dangerous Products into U.S., Protect U.S. Consumers
http://www.fda.gov/news-events/press-announcements/coronavirus-covid-19-update-fda-takes-action-place-all-alcohol-based-hand-sanitizers-mexico-import
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VentStar (N) 180 (2021-01-19)
VentStar (N) 180 (2021-01-19)
https://healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2021/74859r-eng.php
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Vacunas contra la COVID-19
Vacunas contra la COVID-19
https://sites.bvsalud.org/redetsa/brisa/resource/?id=biblioref.referencesource.1146459
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Nostrum Laboratories, Inc. Expands Voluntary Nationwide Recall of Metformin HCl Extended Release Tablets, USP 750 mg, Due to N-Nitrosodimethylamine (NDMA) Content Above the Acceptable Daily Intake (ADI) Limit
Nostrum Laboratories, Inc. is voluntarily recalling one lot of Metformin HCl Extended Release Tablets, USP 750 mg (generic equivalent to Glucophage Tablets) to the consumer level. The Metformin HCl Extended Release Tablets, USP 750 mg (generic equivalent to Glucophage Tablets) have been found to con
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Coronavirus (COVID-19) Update: January 22, 2021
Coronavirus (COVID-19) Update: January 22, 2021
http://www.fda.gov/news-events/press-announcements/coronavirus-covid-19-update-january-22-2021
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Isolation Gown & Kendall Gown (2021-01-11)
Isolation Gown & Kendall Gown (2021-01-11)
https://healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2021/74825r-eng.php
