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Renuvion/J-Plasma device can be used for additional aesthetic skin procedures
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FDA Roundup: May 09, 2023
FDA Roundup: May 09, 2023
http://www.fda.gov/news-events/press-announcements/fda-roundup-may-09-2023
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Cemiplimab (Libtayo®) en carcinoma cutáneo de células escamosas avanzado
Cemiplimab (Libtayo®) en carcinoma cutáneo de células escamosas avanzado
https://sites.bvsalud.org/redetsa/brisa/resource/?id=biblioref.referencesource.1428156
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FDA Roundup: May 05, 2023
FDA Roundup: May 05, 2023
http://www.fda.gov/news-events/press-announcements/fda-roundup-may-05-2023
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Recall Notice – SD Biosensor, Inc. Requests Discontinuation of Use and Disposal of Specific Pilot™ COVID-19 At-Home Tests in the United States Due to Microbial Contamination in the Liquid Buffer Solution
SD Biosensor, Inc. today is requesting that consumers stop using and dispose of specific Pilot COVID-19 At-Home Tests in the United States because potentially harmful bacteria were found in the tube with liquid inside (pouch 2 of the kits). The affected tests can be identified by the lot number on
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Family Dollar is Initiating a Voluntary Recall of Certain Over-the-Counter Drug Products Because the Products Have Been Stored Outside of Labeled Temperature Requirements
Family Dollar is initiating a voluntary retail level product recall of certain over-the-counter drug products regulated by the U.S. Food and Drug Administration (FDA) that were stored and shipped to certain stores on or around June 1, 2022 through March 31, 2023 due to product being stored by Family
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UPDATE – Akorn Issues Voluntary Nationwide Recall of Various Human and Animal Drug Products Within Expiry Due to Company Shutdown
Gurnee, IL, Akorn Operating Company LLC has filed Chapter 7 bankruptcy on February 23, 2023. In connection with that filing, the company has ceased and shutdown all operations and terminated all its employees of all domestic US Sites. The Akorn Trustee is initiating a voluntary recall of various w
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Do Not Use Certain SD Biosensor Pilot COVID-19 At-Home Tests: FDA Safety Communication
Direct contact with the contaminated liquid solution may pose safety concerns and the bacterial contamination could impact the performance of the test.
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Risk of Exposure to Unsafe Levels of Radiation with Safe-T-Lite UV WAND: FDA Safety Communication
Max-Lux Safe-T-Lite UV-C WAND may cause injury to the skin, eyes, or both after a few seconds of use.
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FDA Approves First Respiratory Syncytial Virus (RSV) Vaccine
FDA Approves First Respiratory Syncytial Virus (RSV) Vaccine
http://www.fda.gov/news-events/press-announcements/fda-approves-first-respiratory-syncytial-virus-rsv-vaccine