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FDA Daily

FDA daily for Thursday, October 8, 2026

31 FDA records across 4 sections.

31FDA Records
4 of 7Sections With Data
0Touch MedGrid Categories

Sections in This Issue

Drug shortagesCovers FDA's Wed, Oct 7 (yesterday)
6
  • Felodipine Tablet, Film Coated, Extended Release

    Felodipine, Tablet, Film Coated, Extended Release, 10 mg (NDC 0603-3583-21) — Par Health, USA LLC

    New · To Be Discontinued · Cardiovascular

  • Felodipine Tablet, Extended Release

    Felodipine, Tablet, Extended Release, 2.5 mg (NDC 0603-3581-28) — Par Health, USA LLC

    New · To Be Discontinued · Cardiovascular

  • Felodipine Tablet, Film Coated, Extended Release

    Felodipine, Tablet, Film Coated, Extended Release, 10 mg (NDC 0603-3583-28) — Par Health, USA LLC

    New · To Be Discontinued · Cardiovascular

  • Felodipine Tablet, Extended Release

    Felodipine, Tablet, Extended Release, 2.5 mg (NDC 0603-3581-21) — Par Health, USA LLC

    New · To Be Discontinued · Cardiovascular

  • Felodipine Tablet, Extended Release

    Felodipine, Tablet, Extended Release, 5 mg (NDC 0603-3582-28) — Par Health, USA LLC

    New · To Be Discontinued · Cardiovascular

  • Felodipine Tablet, Extended Release

    Felodipine, Tablet, Extended Release, 5 mg (NDC 0603-3582-21) — Par Health, USA LLC

    New · To Be Discontinued · Cardiovascular

Drug approvalsCovers FDA's Thu, Oct 1 (a week ago)
8
  • ROZLYTREK

    ENTRECTINIB — GENENTECH INC

    NDA212725 · Labeling

  • OLANZAPINE

    OLANZAPINE — SANDOZ INC

    ANDA201588 · Labeling

  • CARBIDOPA AND LEVODOPA

    CARBIDOPA, LEVODOPA — ALEMBIC

    ANDA210341 · Labeling

  • ROZLYTREK

    ENTRECTINIB — GENENTECH INC

    NDA218550 · Labeling

  • NDA219617

    EVER VALINJECT

    NDA219617 · Original approval

  • FENTANYL CITRATE PRESERVATIVE FREE

    FENTANYL CITRATE — FRESENIUS KABI USA

    ANDA210762 · Labeling

  • METHYLPHENIDATE HYDROCHLORIDE

    METHYLPHENIDATE HYDROCHLORIDE — ALVOGEN

    ANDA210818 · Labeling

  • CARBIDOPA AND LEVODOPA

    CARBIDOPA, LEVODOPA — SCIEGEN PHARMS

    ANDA214091 · Labeling

Drug recallsCovers FDA's Thu, Oct 1 (a week ago)
Nothing from FDA for this date
Food and supplement recallsCovers FDA's Thu, Oct 1 (a week ago)
Nothing from FDA for this date
Device recallsCovers FDA's Thu, Oct 1 (a week ago)
Nothing from FDA for this date
Device clearancesCovers FDA's Thu, Sep 24 (two weeks ago)
15
  • Electric Scooter (FNS01,FNS03)

    Anhui Jbh Medical Apparatus Co., Ltd.

    K261078 · Substantially Equivalent · Physical Medicine

  • Disposable Belts for Polysomnography (CNSAC)

    CNSAC Medshop GmbH

    K260949 · Substantially Equivalent · Anesthesiology

  • Arthrex Spine Compression FT Screw

    Arthrex, Inc.

    K262618 · Substantially Equivalent · Unknown

  • KARL STORZ SUPRALOOP

    Karl Storz SE & CO. KG

    K254303 · Substantially Equivalent · Obstetrics/Gynecology

  • Align® Cover and Pad Guidance Tool

    CIVCO Medical Instruments Co., Inc.

    K260114 · Substantially Equivalent · Radiology

  • MPa Max adhesive

    Den-Mat Holdings, LLC

    K262252 · Substantially Equivalent · Dental

  • corra® cervical plating system

    Carlsmed, Inc.

    K262149 · Substantially Equivalent · Orthopedic

  • Pediatric Nailing Platform Femur

    OrthoPediatrics Corp.

    K261345 · Substantially Equivalent · Orthopedic

  • Hair Growth Helmet (TK-176, TK-600, TK-500, TK-282, TK-500A, TK-282A, TK-126, TK-60)

    Shenzhen Nuon Medical Equipment Co., Ltd.

    K262183 · Substantially Equivalent · Physical Medicine

  • ISIS Headboxes, ISIS Neurostimulator, ISIS Xpert Plus, ISIS Xpert, ISIS Xpress

    inomed Medizintechnik GmbH

    K263010 · Substantially Equivalent · Neurology

  • QIAstat-Dx BCID GN Plus AMR Panel

    QIAGEN GmbH

    K262168 · Substantially Equivalent · Microbiology

  • OsseoFit Stemless Shoulder System

    Zimmer, Inc.

    K262955 · Substantially Equivalent · Orthopedic

Showing 12 of 15. Search the rest in openFDA.

Label changesCovers FDA's Thu, Sep 24 (two weeks ago)
2
  • Antifungal Liquid

    Target Corporation

    Label version 2

  • Pharmacys Prescription 4.5 OZ Creamy Petroleum Jelly

    American Consumer Products Corp.

    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.

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.