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FDA Daily

FDA daily for Saturday, August 8, 2026

7 FDA records across 2 sections.

7FDA Records
2 of 7Sections With Data
0Touch MedGrid Categories

Sections in This Issue

Drug shortagesCovers FDA's Fri, Aug 7 (yesterday)
Nothing from FDA for this date
Drug approvalsCovers FDA's Sat, Aug 1 (a week ago)
Nothing from FDA for this date
Drug recallsCovers FDA's Sat, Aug 1 (a week ago)
Nothing from FDA for this date
Food and supplement recallsCovers FDA's Sat, Aug 1 (a week ago)
Nothing from FDA for this date
Device recallsCovers FDA's Sat, Aug 1 (a week ago)
Nothing from FDA for this date
Device clearancesCovers FDA's Sat, Jul 25 (two weeks ago)
2
  • MONARCH™ Platform (MON-000008)

    Auris Health, Inc.

    K260382 · Substantially Equivalent · Ear, Nose, Throat

  • METICULY Patient-specific CMF solution

    Meticuly Co., Ltd.

    K253206 · Substantially Equivalent · Dental

Label changesCovers FDA's Sat, Jul 25 (two weeks ago)
5
  • Rosuvastatin Calcium

    Zhejiang Yongtai Pharmaceutical Co., Ltd.

    Label version 11

  • LUXE COLOR FOUNDATION

    Guangzhou Huixue Biotechnology Co., Ltd.

    Label version 1

  • POSLUMA

    Blue Earth Diagnostics

    Label version 11

  • CVS Topical Anesthetic Hemorrhoidal

    CVS PHARMACY, INC

    Label version 1

  • hydrocortisone

    Eywa Pharma Inc

    Label version 3

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.