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FDA Daily

FDA daily for Tuesday, July 28, 2026

206 FDA records across 4 sections. 4 touch MedGrid's categories and are listed first.

206FDA Records
4 of 7Sections With Data
4Touch MedGrid Categories

Sections in This Issue

Drug shortagesCovers FDA's Mon, Jul 27 (yesterday)
3
  • Fluticasone Propionate and Salmeterol Xinafoate Aerosol, Metered

    Advair HFA, Aerosol, Metered, 230 ug; 21 ug (NDC 0173-0717-22) — GlaxoSmithKline

    New · To Be Discontinued · Pulmonary/Allergy

  • Fluticasone Propionate and Salmeterol Xinafoate Aerosol, Metered

    Advair HFA, Aerosol, Metered, 45 ug; 21 ug (NDC 0173-0715-22) — GlaxoSmithKline

    New · To Be Discontinued · Pulmonary/Allergy

  • Fluticasone Propionate and Salmeterol Xinafoate Aerosol, Metered

    Advair HFA, Aerosol, Metered, 115 ug; 21 ug (NDC 0173-0716-22) — GlaxoSmithKline

    New · To Be Discontinued · Pulmonary/Allergy

Drug approvalsCovers FDA's Tue, Jul 21 (a week ago)
6
  • FLUVOXAMINE MALEATE

    FLUVOXAMINE MALEATE — ZYDUS PHARMS

    ANDA220447 · Original approval

  • CAMCEVI ETM

    LEUPROLIDE MESYLATE — ACCORD

    NDA219745 · Labeling

  • LOPURIN

    ALLOPURINOL — DR REDDYS

    ANDA071587 · Labeling

  • PITOLISANT HYDROCHLORIDE

    PITOLISANT HYDROCHLORIDE — NOVITIUM PHARMA

    ANDA218495 · Original approval

  • BUPROPION HYDROCHLORIDE

    BUPROPION HYDROCHLORIDE — AUROBINDO PHARMA LTD

    ANDA216051 · Original approval

  • TOLVAPTAN

    TOLVAPTAN — TEVA PHARMS INC

    ANDA216933 · Original approval

Drug recallsCovers FDA's Tue, Jul 21 (a week ago)
Nothing from FDA for this date
Food and supplement recallsCovers FDA's Tue, Jul 21 (a week ago)
Nothing from FDA for this date
Device recallsCovers FDA's Tue, Jul 21 (a week ago)
Nothing from FDA for this date
Device clearancesCovers FDA's Tue, Jul 14 (two weeks ago)
8
  • Universal Seal (5-12 mm)

    Intuitive Surgical, Inc.

    K261249 · Substantially Equivalent · Gastroenterology, Urology

  • Symmetrix™ L Spinal System

    Medtronic Sofamor Danek USA, Inc.

    K261020 · Substantially Equivalent · Orthopedic

  • LIXI (LXOSFM1)

    Luwi, LLC

    K253662 · Substantially Equivalent · Obstetrics/Gynecology

  • Invictus® Small Stature Spinal Fixation System; Invictus® 2.0 Spinal Fixation System

    Alphatec Spine, Inc.

    K261284 · Substantially Equivalent · Orthopedic

  • IERO Mobility Scooter (IERO-01)

    Jochu Technology Co., Ltd.

    K261232 · Substantially Equivalent · Physical Medicine

  • Accoat Guide Wire

    Sp Medical A/S

    K253667 · Substantially Equivalent · Cardiovascular

  • VisuBreath

    Affirm Medical Technologies II, LLC

    K261633 · Substantially Equivalent · Anesthesiology

  • Ambu® NeurolineTM Cup MRI/CT (Models 72704/21US, 72704/23US, 72704/25US, 72704/27US) Ambu® NeurolineTM Cup MRI/CT-set (…

    Ambu A/S

    K260578 · Substantially Equivalent · Neurology

Label changesCovers FDA's Tue, Jul 14 (two weeks ago)
4 touch MedGrid189
  • Zinc Oxide Perfecting SunscreenTouches MedGrid categories

    Epicuren Discovery

    Label version 2

  • Testosterone CypionateTouches MedGrid categories

    Bryant Ranch Prepack

    Label version 101

  • X-Treme Cream Propolis Sunscreen SPF 45Touches MedGrid categories

    Epicuren Discovery

    Label version 3

  • Lidocaine Numbing CreamTouches MedGrid categories

    KORVIA GLOBAL Inc.

    Label version 1

  • Trazodone Hydrochloride

    A-S Medication Solutions

    Label version 4

  • Drug label

    Label version 5

  • Remedy Barrier Cream Cloths Fragrance Free

    Medline Industries, LP

    Label version 12

  • Modafinil

    Preferred Pharmaceuticals Inc.

    Label version 4

  • Drug label

    Label version 3

  • Lurasidone Hydrochloride

    Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.

    Label version 7

  • Drug label

    Label version 1

  • Felbamate

    Sun Pharmaceutical Industries, Inc.

    Label version 4

Showing 12 of 189. 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.