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FDA Daily

FDA daily for Sunday, August 16, 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 Sat, Aug 15 (yesterday)
Nothing from FDA for this date
Drug approvalsCovers FDA's Sun, Aug 9 (a week ago)
1
  • NITROUS OXIDE, USP

    NITROUS OXIDE — LINDE GAS EQUIP

    NDA221892 · Original approval

Drug recallsCovers FDA's Sun, Aug 9 (a week ago)
Nothing from FDA for this date
Food and supplement recallsCovers FDA's Sun, Aug 9 (a week ago)
Nothing from FDA for this date
Device recallsCovers FDA's Sun, Aug 9 (a week ago)
Nothing from FDA for this date
Device clearancesCovers FDA's Sun, Aug 2 (two weeks ago)
Nothing from FDA for this date
Label changesCovers FDA's Sun, Aug 2 (two weeks ago)
6
  • Rocuronium

    Fresenius Kabi USA, LLC

    Label version 1

  • JOHNSON FOAM

    JOHNSON BIOPHARMACEUTICAL INC.

    Label version 8

  • JOHNSON FOAM PRO

    JOHNSON BIOPHARMACEUTICAL INC.

    Label version 5

  • Wart Remover

    Shantou South Moon Biotechnology Co., Ltd.

    Label version 2

  • Drug label

    Label version 2

  • BBlove Hand Sanitizer Fresh Squeezed Spearmint

    Shenzhen Lantern Scicence Co.,Ltd.

    Label version 1

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.