FDA daily for Saturday, October 3, 2026
172 FDA records across 3 sections. 8 touch MedGrid's categories and are listed first.
Drug shortagesCovers FDA's Fri, Oct 2 (yesterday)8 touch MedGrid168
- Lidocaine Hydrochloride InjectionTouches MedGrid categories
Lidocaine Hydrochloride, Injection, 20 mg/mL (NDC 55150-164-02) — Eugia US LLC
- Lidocaine Hydrochloride InjectionTouches MedGrid categories
Lidocaine Hydrochloride, Injection, 10 mg/mL (NDC 55150-251-10) — Eugia US LLC
- Lidocaine Hydrochloride InjectionTouches MedGrid categories
Lidocaine Hydrochloride, Injection, 10 mg/1 mL (NDC 55150-163-30) — Eugia US LLC
- Lidocaine Hydrochloride InjectionTouches MedGrid categories
Lidocaine Hydrochloride And Dextrose, Injection, 8 mg/1 mL (NDC 0338-0411-02) — Baxter Healthcare
- Lidocaine Hydrochloride InjectionTouches MedGrid categories
Lidocaine Hydrochloride, Injection, 20 mg/1 mL (NDC 55150-165-05) — Eugia US LLC
- Lidocaine Hydrochloride InjectionTouches MedGrid categories
Lidocaine Hydrochloride, Injection, 20 mg/mL (NDC 55150-255-20) — Eugia US LLC
- Lidocaine Hydrochloride InjectionTouches MedGrid categories
Lidocaine Hydrochloride, Injection, 10 mg/mL (NDC 55150-252-20) — Eugia US LLC
- Lidocaine Hydrochloride InjectionTouches MedGrid categories
Lidocaine Hydrochloride, Injection, 10 mg/1 mL (NDC 55150-161-02) — Eugia US LLC
- Dextrose Monohydrate 5% Injection
Dextrose 5% In Plastic Container, Injection, 50 g/1000 mL (NDC 0338-0017-48) — Baxter Healthcare
- Dexmedetomidine Hydrochloride Injection
Dexmedetomidine Hydrochloride, Injection, 4 ug/1 mL (NDC 55150-296-10) — Eugia US LLC
- Amphetamine Aspartate Monohydrate, Amphetamine Sulfate, Dextroamphetamine Saccharate, Dextroamphetamine Sulfate Tablet
Amphetamine Aspartate Monohydrate, Amphetamine Sulfate, Dextroamphetamine Saccharate, Dextroamphetamine Sulfate, Tablet, 15mg (NDC 47781-178-01) — Alvogen
- Lisdexamfetamine Dimesylate Capsule
Lisdexamfetamine Dimesylate, Capsule, 50 mg (NDC 64850-554-01) — Elite Laboratories, Inc.
Showing 12 of 168. Search the rest in openFDA.
Device clearancesCovers FDA's Sat, Sep 19 (two weeks ago)3
- SmartIPL_NI System
Lumenis Be, Ltd.
- Electric Scooter (FDB08, FDB08A, FDB12)
Anhui JBH Medical Apparatus Co., Ltd.
- Dynamis Pro Family
Fotona D.O.O.
Label changesCovers FDA's Sat, Sep 19 (two weeks ago)1
- QKEKL RINGWORM TREATMENT
Guangzhou Huixue Biotechnology Co., Ltd.
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.