Skip to content
Physician-backed infrastructure for aesthetic & wellness practicesSupport 9 AM–5 PM EST ·(888) 996-6173 ·info@medgrid.com
MedGrid
FDA Daily

FDA daily for Tuesday, September 1, 2026

30 FDA records across 3 sections. 2 touch MedGrid's categories and are listed first.

FDA did not answer for Label changes while this issue was written; those sections will fill in on a later visit.

30FDA Records
3 of 6Sections With Data
2Touch MedGrid Categories

Sections in This Issue

Drug shortagesCovers FDA's Mon, Aug 31 (yesterday)
2 touch MedGrid11
  • Medroxyprogesterone Acetate TabletTouches MedGrid categories

    PROVERA, Tablet, 10 mg (NDC 0009-0051-01) — Pfizer Inc.

    New · To Be Discontinued · Urology

  • Medroxyprogesterone Acetate TabletTouches MedGrid categories

    PROVERA, Tablet, 2.5 mg (NDC 0009-0065-01) — Pfizer Inc.

    New · To Be Discontinued · Urology

  • Metoprolol Succinate Tablet, Extended Release

    Metoprolol Succinate, Tablet, Extended Release, 50 mg (NDC 45963-676-11) — Teva Pharmaceuticals USA, Inc.

    New · To Be Discontinued · Cardiovascular

  • Metoprolol Succinate Tablet, Extended Release

    Metoprolol Succinate, Tablet, Extended Release, 100 mg (NDC 45963-677-11) — Teva Pharmaceuticals USA, Inc.

    New · To Be Discontinued · Cardiovascular

  • Metoprolol Succinate Tablet, Extended Release

    Metoprolol Succinate, Tablet, Extended Release, 25 mg (NDC 45963-709-96) — Teva Pharmaceuticals USA, Inc.

    New · To Be Discontinued · Cardiovascular

  • Metoprolol Succinate Tablet, Extended Release

    Metoprolol Succinate, Tablet, Extended Release, 25 mg (NDC 45963-709-11) — Teva Pharmaceuticals USA, Inc.

    New · To Be Discontinued · Cardiovascular

  • Metoprolol Succinate Tablet, Extended Release

    Metoprolol Succinate, Tablet, Extended Release, 200 mg (NDC 45963-678-11) — Teva Pharmaceuticals USA, Inc.

    New · To Be Discontinued · Cardiovascular

  • Metoprolol Succinate Tablet, Extended Release

    Metoprolol Succinate, Tablet, Extended Release, 50 mg (NDC 45963-676-96) — Teva Pharmaceuticals USA, Inc.

    New · To Be Discontinued · Cardiovascular

  • Potassium Chloride, Sodium Chloride, Calcium Chloride, and Magnesium Chloride Injection, Solution

    Cardioplegic Solution, Injection, Solution, 17.6 mg/100 mL; 325.3 mg/100 mL; 119.3 mg/100 mL; 643 mg/100 mL (NDC 65219-258-10) — Fresenius Kabi USA, LLC

    New · To Be Discontinued · Cardiovascular

  • Palovarotene Capsule

    SOHONOS, Capsule, 2.5 mg (NDC 15054-0025-1) — Ipsen Biopharmaceuticals, Inc.

    New · To Be Discontinued · Musculoskeletal

  • Metoprolol Succinate Tablet, Extended Release

    Metoprolol Succinate, Tablet, Extended Release, 100 mg (NDC 45963-677-96) — Teva Pharmaceuticals USA, Inc.

    New · To Be Discontinued · Cardiovascular

Drug approvalsCovers FDA's Tue, Aug 25 (a week ago)
9
  • FLUTICASONE PROPIONATE

    FLUTICASONE PROPIONATE — AUROBINDO PHARMA LTD

    ANDA217088 · Labeling

  • ZIIHERA

    ZANIDATAMAB-HRII — JAZZ PHARMS

    BLA761416 · Efficacy

  • TADALAFIL

    TADALAFIL — SUN PHARM

    ANDA208934 · Manufacturing (CMC)

  • METOPROLOL SUCCINATE

    METOPROLOL SUCCINATE — HETERO LABS LTD III

    ANDA205541 · Labeling

  • TIVICAY

    DOLUTEGRAVIR SODIUM — VIIV HLTHCARE

    NDA204790 · Efficacy

  • TIVICAY PD

    DOLUTEGRAVIR SODIUM — VIIV HLTHCARE

    NDA213983 · Efficacy

  • GABAPENTIN

    GABAPENTIN — RUBICON RESEARCH

    ANDA216492 · Labeling

  • TEVIMBRA

    TISLELIZUMAB-JSGR — BEIGENE

    BLA761232 · Efficacy

  • ISOPROTERENOL HYDROCHLORIDE

    ISOPROTERENOL HYDROCHLORIDE — EUGIA PHARMA

    ANDA211864 · Labeling

Drug recallsCovers FDA's Tue, Aug 25 (a week ago)
Nothing from FDA for this date
Food and supplement recallsCovers FDA's Tue, Aug 25 (a week ago)
Nothing from FDA for this date
Device recallsCovers FDA's Tue, Aug 25 (a week ago)
Nothing from FDA for this date
Device clearancesCovers FDA's Tue, Aug 18 (two weeks ago)
10
  • BluEX Cervical Expandable Cage System

    L&K BIOMED Co., Ltd.

    K262489 · Substantially Equivalent · Orthopedic

  • Lancing device

    Tianjin Huahong Technology Co., Ltd.

    K262135 · Substantially Equivalent · General, Plastic Surgery

  • TearCare System

    Sight Sciences, Inc.

    K262479 · Substantially Equivalent · Ophthalmic

  • Tympendi™ (810)

    Grace Medical, Inc.

    K260266 · Substantially Equivalent · Ear, Nose, Throat

  • NON-STERILE POWDER FREE NITRILE PATIENT EXAMINATION GLOVES, WITH LICORICE ROOT EXTRACT AND UREA, TESTED FOR USE WITH CH…

    Kossan International Sdn Bhd

    K260794 · Substantially Equivalent · General Hospital

  • TeKBrace Solo Soft Tissue Reinforcement Device

    Theramicro

    K262729 · Substantially Equivalent · General, Plastic Surgery

  • LUOFUCON® Wound Matrix

    Huizhou Foryou Medical Devices Co., Ltd.

    K254256 · Substantially Equivalent · Unknown

  • Lower Limb AI (LLAI)

    AI Planning Logic, Inc.

    K261641 · Substantially Equivalent · Radiology

  • p17 XR Microcatheter

    Wallaby Medical

    K254071 · Substantially Equivalent · Cardiovascular

  • HERizon RD5 Resecting Device (5FR1PK);HERizon RD5 Resecting Device - 5 pack (5FR5PK)

    Axora Medical, Inc.

    K260984 · Substantially Equivalent · Obstetrics/Gynecology

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.

Subscribe with any feed reader, or point an email tool at theRSS feed. For the rules behind the headlines, see Regulations Research.

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.