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FDA Daily

FDA daily for Sunday, August 2, 2026

7 FDA records across 1 section.

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

Sections in This Issue

Drug shortagesCovers FDA's Sat, Aug 1 (yesterday)
Nothing from FDA for this date
Drug approvalsCovers FDA's Sun, Jul 26 (a week ago)
Nothing from FDA for this date
Drug recallsCovers FDA's Sun, Jul 26 (a week ago)
Nothing from FDA for this date
Food and supplement recallsCovers FDA's Sun, Jul 26 (a week ago)
Nothing from FDA for this date
Device recallsCovers FDA's Sun, Jul 26 (a week ago)
Nothing from FDA for this date
Device clearancesCovers FDA's Sun, Jul 19 (two weeks ago)
Nothing from FDA for this date
Label changesCovers FDA's Sun, Jul 19 (two weeks ago)
7
  • Meijer Antibacterial Spring Rain Hand

    Meijer, Inc.

    Label version 2

  • Biopure 70% Isopropyl Alcohol Wipe

    QUEST USA CORP

    Label version 2

  • hand sanitizer 01

    Cosmuses Cosmetics (Ningbo) Co., Ltd.

    Label version 2

  • TOCOBO Double UV Defense Set

    PICTON Co., Ltd.

    Label version 2

  • 5%MINOXIDIL TOPICAL FOAM

    Veloce Trading Co., Limited

    Label version 1

  • Urgent First Aid BZK Antiseptic Wipe

    Changzhou Maokang Medical Products Co., Ltd

    Label version 1

  • Green Antibacterial Dish and HandSoap

    Meijer, Inc.

    Label version 4

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.