FDA daily

FDA daily for Tuesday, September 8, 2026

In this issue: 8 approvals, 4 device recalls, 16 device decisions and 152 label changes. 3 items touch categories MedGrid carries, and they come first.

For MedGrid's categories

Items in this issue that name a product category sold on MedGrid. Each links to its full FDA record; the chip opens that category's federal and state rules.

Drug and biologic approvals

FDA date:

On Tue, Sep 1 FDA approved no new applications and 8 supplements to existing ones.

Browse drug and biologic approvals in FDA data →

Device recalls

FDA date:

FDA posted 4 device recalls from 1 firm on Tue, Sep 1.

Browse device recalls in FDA data →

Device clearances and approvals

FDA date:

FDA decided 10 510(k)s and 6 PMA decisions on Tue, Aug 25.

Browse device clearances and approvals in FDA data →

Label updates

FDA date:

152 drug labels took effect on Tue, Aug 25; 1 of the 25 read for this issue is for products in MedGrid's categories. Below: those, and labels carrying a boxed warning.

  • Minoxidil

    MINOXIDIL · American Health Packaging · ORAL

    Topical hair lossBoxed warningHUMAN PRESCRIPTION DRUG
  • Synjardy

    EMPAGLIFLOZIN AND METFORMIN HYDROCHLORIDE · Boehringer Ingelheim Pharmaceuticals, Inc. · ORAL

    Boxed warningHUMAN PRESCRIPTION DRUG
  • alogliptin and metformin hydrochloride

    ALOGLIPTIN AND METFORMIN HYDROCHLORIDE · Padagis Israel Pharmaceuticals Ltd · ORAL

    Boxed warningHUMAN PRESCRIPTION DRUG
  • Depo-Provera

    MEDROXYPROGESTERONE ACETATE · Pharmacia & Upjohn Company LLC · INTRAMUSCULAR

    Boxed warningHUMAN PRESCRIPTION DRUG
  • Hydrocodone Bitartrate and Homatropine Methylbromide

    HYDROCODONE BITARTRATE AND HOMATROPINE METHYLBROMIDE · KVK-Tech, Inc. · ORAL

    Boxed warningHUMAN PRESCRIPTION DRUG
Browse label updates in FDA data →

FDA did not answer for Food and supplement recalls, Drug shortages, Drug recalls while this issue was written; those sections will fill in on a later visit.

How the FDA daily is written

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 and 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. Complete response letters appear the day after FDA publishes a batch.

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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.