FDA daily for Saturday, August 22, 2026
11 FDA records across 1 section. 2 touch MedGrid's categories and are listed first.
Label changesCovers FDA's Sat, Aug 8 (two weeks ago)2 touch MedGrid11
- Gniby LIDOCAINE ANORECTAL HEMORRHOIDAL NumbingTouches MedGrid categories
Putian Licheng District Zhijiancheng Trading Co., Ltd.
- ORLASKIN SPF50 Antioxidant SoothingComplex SunscreenTouches MedGrid categories
Guangzhou Yapheon Health Industry Co., Ltd.
- Sodium Sulfate, Potassium Sulfate and Magnesium Sulfate
Ascend Laboratories, LLC
- antibacterial hand wipes (JUICY WATERMELON)
Zhejiang Furuisen Spunlaced Nonwovens Co., Ltd.
- SPESOLSKII WART CORN CALLUS REMOVER
BEST GREEN LIMITED
- APUREE Prorevive Maximum Strength Antifungal
Guangzhou Meixi Biotechnology Co., Ltd.
- Skin Wart Remover Liquid
Shenzhen Earth Surface Trading Co., Ltd.
- TERAZOSIN HYDROCHLORIDE
Apnar Pharma LP
- Sucralfate
Zydus Lifesciences Limited
- Relieve and Relax Pain Relieving
MAC Innovations, LLC
- Sucralfate
Viona Pharmaceuticals Inc
How the FDA Daily Is WrittenSources, dates and what gets flagged
Every issue is written from FDA's public data (openFDA) and nothing else: the counts, names, firms and reasons are FDA's own. openFDA posts each kind of record on its own delay, so each section covers one FDA date and says which. Shortages cover yesterday; approvals, drug recalls, device recalls and food and supplement recalls cover a week ago; device clearances and label changes cover two weeks ago. Every FDA date appears in exactly one issue. Items that touch the categories MedGrid works in, such as GLP-1s, hormones, injectables, peptides, compounded products and aesthetic devices, are marked and listed first.
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Data from openFDA, FDA's public API. FDA says not to rely on it to make decisions about medical care and to treat every result as unvalidated; confirm against FDA's own record and the product labeling. Not medical or legal advice.