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FDA Daily

FDA daily for Sunday, August 30, 2026

14 FDA records across 2 sections. 2 touch MedGrid's categories and are listed first.

14FDA Records
2 of 7Sections With Data
2Touch MedGrid Categories

Sections in This Issue

Drug shortagesCovers FDA's Sat, Aug 29 (yesterday)
Nothing from FDA for this date
Drug approvalsCovers FDA's Sun, Aug 23 (a week ago)
Nothing from FDA for this date
Drug recallsCovers FDA's Sun, Aug 23 (a week ago)
Nothing from FDA for this date
Food and supplement recallsCovers FDA's Sun, Aug 23 (a week ago)
Nothing from FDA for this date
Device recallsCovers FDA's Sun, Aug 23 (a week ago)
Nothing from FDA for this date
Device clearancesCovers FDA's Sun, Aug 16 (two weeks ago)
1
  • CN-Suite™

    FIND Surgical Sciences Inc. D/B/A FIND Neuro

    K260563 · Substantially Equivalent · Neurology

Label changesCovers FDA's Sun, Aug 16 (two weeks ago)
2 touch MedGrid13
  • Sun Zapper - Acne Pure Zinc Sunscreen SPF50Touches MedGrid categories

    Veganic SKN Limited

    Label version 3

  • Sun Zapper - Anti-ageing pure zinc sunscreen SPF30Touches MedGrid categories

    VEGANIC SKN LIMITED

    Label version 3

  • Drug label

    Label version 2

  • Daytime Nighttime

    KROGER COMPANY

    Label version 6

  • WISH HAND SANITIZER Sea Salt Green Herbs

    PT SUPER HOME PRODUCT INDONESIA

    Label version 1

  • WISH HAND SANITIZER Marshmallow Vanilla

    PT SUPER HOME PRODUCT INDONESIA

    Label version 1

  • WISH HAND SANITIZER Lychee Vanilla Milk

    PT SUPER HOME PRODUCT INDONESIA

    Label version 1

  • ATOMY ANTICAVITY TOOTH

    ATOMY CO., LTD.

    Label version 1

  • Hydrocortisone with Aloe

    Sun Pharmaceutical Industries, Inc.

    Label version 1

  • PUTRIZEN ARNICA BRUISE RELIEF Cream

    GUANGZHOU YUSONG FINE CHEMICLS Co., Ltd

    Label version 1

  • SIERQ Numbing

    Putian Licheng District Zhijiancheng Trading Co., Ltd.

    Label version 1

  • Lithium Carbonate

    Hikma Pharmaceuticals USA Inc.

    Label version 3

Showing 12 of 13. Search the rest in openFDA.

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.